HYDRODERM GEL WOUND DRESSING
K-Number: K944333 · 1994-11-10
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Device Summary
Frequently Asked Questions
What is the HYDRODERM GEL WOUND DRESSING?
HYDRODERM GEL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1994-11-10. The listed applicant is Wilshire Medical Products. The 510(k) number is K944333.
When did HYDRODERM GEL WOUND DRESSING receive FDA 510(k) clearance?
HYDRODERM GEL WOUND DRESSING received FDA 510(k) clearance on 1994-11-10, under 510(k) number K944333.
Who is the listed applicant for HYDRODERM GEL WOUND 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 HYDRODERM GEL WOUND DRESSING?
The FDA product code for HYDRODERM GEL 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 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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