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FDA 510(k)

MODIFICATION TO WOUN'DRES

K-Number: K991202 · 1999-06-04

ApplicantColoplast Corp.
Decision Date1999-06-04
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO WOUN'DRES is the device name listed in this FDA 510(k) record. The listed applicant is Coloplast Corp.. It received FDA 510(k) clearance on 1999-06-04 under 510(k) number K991202. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO WOUN'DRES?

MODIFICATION TO WOUN'DRES is a medical device that received FDA 510(k) clearance on 1999-06-04. The listed applicant is Coloplast Corp.. The 510(k) number is K991202.

When did MODIFICATION TO WOUN'DRES receive FDA 510(k) clearance?

MODIFICATION TO WOUN'DRES received FDA 510(k) clearance on 1999-06-04, under 510(k) number K991202.

Who is the listed applicant for MODIFICATION TO WOUN'DRES?

The FDA 510(k) record lists Coloplast Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO WOUN'DRES?

The FDA product code for MODIFICATION TO WOUN'DRES is MGQ.

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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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