DERMASSIST(TM) HYDROGEL SATURATEED NON WOVEN DRESSING
K-Number: K946031 · 1995-02-27
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Device Summary
Frequently Asked Questions
What is the DERMASSIST(TM) HYDROGEL SATURATEED NON WOVEN DRESSING?
DERMASSIST(TM) HYDROGEL SATURATEED NON WOVEN DRESSING is a medical device that received FDA 510(k) clearance on 1995-02-27. The listed applicant is Wilshire Medical Products. The 510(k) number is K946031.
When did DERMASSIST(TM) HYDROGEL SATURATEED NON WOVEN DRESSING receive FDA 510(k) clearance?
DERMASSIST(TM) HYDROGEL SATURATEED NON WOVEN DRESSING received FDA 510(k) clearance on 1995-02-27, under 510(k) number K946031.
Who is the listed applicant for DERMASSIST(TM) HYDROGEL SATURATEED NON WOVEN DRESSING?
The FDA 510(k) record lists Wilshire Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DERMASSIST(TM) HYDROGEL SATURATEED NON WOVEN DRESSING?
The FDA product code for DERMASSIST(TM) HYDROGEL SATURATEED NON WOVEN DRESSING is MGQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Wilshire Medical Products as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MGQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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