Premd, Inc.
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- Devices
- 1
What Premd, Inc. makes
Premd, Inc. manufactures the PREVU Point of Care Skin Sterol Test, a diagnostic device designed for on-site measurement of skin sterol levels to aid in clinical assessments.
The PREVU Point of Care Skin Sterol Test is classified as a Class I device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Prevu Point Of Care Skin Sterol Test Ref K062092
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Premd, Inc. have in the registry?
The registry currently lists 1 device for Premd, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Premd, Inc.'s devices?
Among its 1 most recently registered device, Premd, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Premd, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Premd, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Premd, Inc. in the registry?
The most recently registered devices listed for Premd, Inc. include PREVU POINT OF CARE SKIN STEROL TEST.