MPM REGENECARE WOUND GEL
K-Number: K992074 · 1999-12-23
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Device Summary
Frequently Asked Questions
What is the MPM REGENECARE WOUND GEL?
MPM REGENECARE WOUND GEL is a medical device that received FDA 510(k) clearance on 1999-12-23. The listed applicant is Mpm Medical., Inc.. The 510(k) number is K992074.
When did MPM REGENECARE WOUND GEL receive FDA 510(k) clearance?
MPM REGENECARE WOUND GEL received FDA 510(k) clearance on 1999-12-23, under 510(k) number K992074.
Who is the listed applicant for MPM REGENECARE WOUND GEL?
The FDA 510(k) record lists Mpm Medical., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MPM REGENECARE WOUND GEL?
The FDA product code for MPM REGENECARE WOUND GEL 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 Mpm Medical., Inc. 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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