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FDA 510(k)

MEDLINE TENDER WET WOUND DRESSING

K-Number: K991755 · 2000-04-17

ApplicantMedline Industries, Inc.
Decision Date2000-04-17
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

MEDLINE TENDER WET WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2000-04-17 under 510(k) number K991755. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE TENDER WET WOUND DRESSING?

MEDLINE TENDER WET WOUND DRESSING is a medical device that received FDA 510(k) clearance on 2000-04-17. The listed applicant is Medline Industries, Inc.. The 510(k) number is K991755.

When did MEDLINE TENDER WET WOUND DRESSING receive FDA 510(k) clearance?

MEDLINE TENDER WET WOUND DRESSING received FDA 510(k) clearance on 2000-04-17, under 510(k) number K991755.

Who is the listed applicant for MEDLINE TENDER WET WOUND DRESSING?

The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDLINE TENDER WET WOUND DRESSING?

The FDA product code for MEDLINE TENDER WET WOUND DRESSING is MGQ.

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Related Devices (Code: 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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