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FDA 510(k)

L.A.M. IPM WOUND GEL

K-Number: K020325 · 2002-04-15

ApplicantL.A.M. Pharmaceutical, Corp.
Decision Date2002-04-15
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

L.A.M. IPM WOUND GEL is the device name listed in this FDA 510(k) record. The listed applicant is L.A.M. Pharmaceutical, Corp.. It received FDA 510(k) clearance on 2002-04-15 under 510(k) number K020325. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L.A.M. IPM WOUND GEL?

L.A.M. IPM WOUND GEL is a medical device that received FDA 510(k) clearance on 2002-04-15. The listed applicant is L.A.M. Pharmaceutical, Corp.. The 510(k) number is K020325.

When did L.A.M. IPM WOUND GEL receive FDA 510(k) clearance?

L.A.M. IPM WOUND GEL received FDA 510(k) clearance on 2002-04-15, under 510(k) number K020325.

Who is the listed applicant for L.A.M. IPM WOUND GEL?

The FDA 510(k) record lists L.A.M. Pharmaceutical, Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L.A.M. IPM WOUND GEL?

The FDA product code for L.A.M. IPM WOUND GEL is MGQ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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