Polymedica Pharmaceuticals, U.S.A., Inc.]
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- Devices
- 1
What Polymedica Pharmaceuticals, U.S.A., Inc.] makes
Polymedica Pharmaceuticals manufactures the Liberty Blood Glucose Monitoring System, a device designed for continuous or intermittent blood glucose level measurement in diabetic patients.
The Liberty Blood Glucose Monitoring System is classified as a Class II medical device under U.S. regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Liberty Blood Glucose Monitoring System Ref K014167
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Polymedica Pharmaceuticals, U.S.A., Inc.] have in the registry?
The registry currently lists 1 device for Polymedica Pharmaceuticals, U.S.A., Inc.]. Devices recorded under merged duplicate company entries are counted once.
Which registries list Polymedica Pharmaceuticals, U.S.A., Inc.]'s devices?
Among its 1 most recently registered device, Polymedica Pharmaceuticals, U.S.A., Inc.] has devices listed in FDA 510(k) (1 device).
What risk classes do Polymedica Pharmaceuticals, U.S.A., Inc.]'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Polymedica Pharmaceuticals, U.S.A., Inc.]'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Polymedica Pharmaceuticals, U.S.A., Inc.] in the registry?
The most recently registered devices listed for Polymedica Pharmaceuticals, U.S.A., Inc.] include LIBERTY BLOOD GLUCOSE MONITORING SYSTEM.