- FDA issues recall notice on Nova strips. Newman, Elizabeth // McKnight's Long-Term Care News;Sep2013, Vol. 34 Issue 9, p20
The article informs that the U.S. Food and Drug Administration has advised to monitor nursing facilities residents for recalled blood glucose test strips marketed as Nova Max Blood Glucose Test Strips or Nova Max Plus Glucose Meter Kits which might report a false high blood glucose result.
- Reverse iontophoresis for monitoring blood glucose. Saunders, Carol S. // Patient Care;2/15/2000, Vol. 34 Issue 3, p14
Reports on the United States Food and Drug Administration Clinical Chemistry and Clinical Toxicology Devices Panel's approval of a noninvasive blood glucose-monitoring biographer called GlucoWatch. Cygnus Inc. as manufacturer of the product; Product's reduction of finger sticks.
- Medtronic's wireless glucose meter receives okay from FDA. Yoffee, Lynn // Diagnostics & Imaging Week;5/8/2008, Vol. 11 Issue 19, p1
The article reports that the U.S. Food and Drug Administration (FDA) has cleared the OneTouch Ultralink glucose meter from Medtronic. The meter transmits glucose readings directly to the company's MiniMed Paradigm insulin pumps and the Guardian Realtime Continuous Monitoring System. The device...
- The Year of the Meter. Mendosa, David // Diabetes Health;Jul2006, Vol. 15 Issue 7, p43
The article focuses on blood glucose meter and blood glucose sensors. Accu-Chek Compact Plus was launched by Roche Diagnostics. The sensors are called episodic meters by Audrey Finkelstein, executive vice president of marketing, sales and clinical affairs for Animas Corp. The STS continuous...
- Despite roadblocks Luminous still in 510(k) path with glucose monitor. Ford, Omar // Medical Device Daily;10/19/2009, Vol. 13 Issue 201, p1
The article reports on the difficulties being experienced by Luminous to obtain a 501(k) approval for its glucose monitoring technology from the U.S. Food and Drug Administration (FDA). According to the FDA, the technology is not something they have dealt with before and they are not quite so...
- Product Briefs. // Medical Device Daily;8/6/2012, Vol. 16 Issue 151, p7
The article reports on the approval being sought by Philosys from the U.S. Food and Drug Administration (FDA) for its Gmate blood glucose monitoring system.
- SweetSpot gets FDA clearance for diabetes data management. // Medical Device Daily;11/30/2011, Vol. 15 Issue 228, p4
The article reports that clearance has been issued by the U.S. Food and Drug Administration (FDA) to SweetSpot Diabetes Care for the SweetSpot Diabetes Data Management Service that will help understand and use of data from blood glucose meters for the diagnosis and management of diabetes.
- Some say two glucose sensors are a 'marginal' gain over one. McCARTY, MARK // Medical Device Daily;6/30/2011, Vol. 15 Issue 121, p1
The article discusses glucose sensors, highlighting the latest trends on the development of such devices used in the treatment of diabetes. It focuses on the current debate on the use of two sensors versus a single sensor in measuring glucose levels, noting that the U.S. Food and Drug...
- Diabetics may no longer need to do finger sticks. Moore, Amy Slugg // RN;Mar99, Vol. 62 Issue 3, p18
Reports on the United States Food and Drug Administration's approval of a device that enables diabetics to check their blood sugar levels at home without using a lancet. Features of the product called Personal Lasette; Manufacture of device by Cell Robotics Inc.