AQUAFLO BTP HYDROGEL WOUND DRESSING
K-Number: K952938 · 1995-12-08
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Device Summary
Frequently Asked Questions
What is the AQUAFLO BTP HYDROGEL WOUND DRESSING?
AQUAFLO BTP HYDROGEL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1995-12-08. The listed applicant is Sherwood Medical Co.. The 510(k) number is K952938.
When did AQUAFLO BTP HYDROGEL WOUND DRESSING receive FDA 510(k) clearance?
AQUAFLO BTP HYDROGEL WOUND DRESSING received FDA 510(k) clearance on 1995-12-08, under 510(k) number K952938.
Who is the listed applicant for AQUAFLO BTP HYDROGEL WOUND DRESSING?
The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AQUAFLO BTP HYDROGEL WOUND DRESSING?
The FDA product code for AQUAFLO BTP HYDROGEL WOUND 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 Sherwood Medical Co. 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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