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FDA 510(k)

MPM HYDROGEL SATURATED DRESSING

K-Number: K930560 · 1993-07-08

Decision Date1993-07-08
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

MPM HYDROGEL SATURATED DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Mpm Medical., Inc.. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K930560. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MPM HYDROGEL SATURATED DRESSING?

MPM HYDROGEL SATURATED DRESSING is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Mpm Medical., Inc.. The 510(k) number is K930560.

When did MPM HYDROGEL SATURATED DRESSING receive FDA 510(k) clearance?

MPM HYDROGEL SATURATED DRESSING received FDA 510(k) clearance on 1993-07-08, under 510(k) number K930560.

Who is the listed applicant for MPM HYDROGEL SATURATED DRESSING?

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 SATURATED DRESSING?

The FDA product code for MPM HYDROGEL SATURATED 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 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.

View all 9 devices →

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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