MPM HYDROGEL
K-Number: K942798 · 1994-07-11
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Device Summary
Frequently Asked Questions
What is the MPM HYDROGEL?
MPM HYDROGEL is a medical device that received FDA 510(k) clearance on 1994-07-11. The listed applicant is Mpm Medical., Inc.. The 510(k) number is K942798.
When did MPM HYDROGEL receive FDA 510(k) clearance?
MPM HYDROGEL received FDA 510(k) clearance on 1994-07-11, under 510(k) number K942798.
Who is the listed applicant for MPM HYDROGEL?
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 HYDROGEL?
The FDA product code for MPM HYDROGEL 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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