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FDA 510(k)

KERLIX MD ANTIMICROBIAL GAUZE DRESSING

K-Number: K990530 · 2000-01-31

ApplicantThe Kendall Company, L.P.
Decision Date2000-01-31
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KERLIX MD ANTIMICROBIAL GAUZE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is The Kendall Company, L.P.. It received FDA 510(k) clearance on 2000-01-31 under 510(k) number K990530. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KERLIX MD ANTIMICROBIAL GAUZE DRESSING?

KERLIX MD ANTIMICROBIAL GAUZE DRESSING is a medical device that received FDA 510(k) clearance on 2000-01-31. The listed applicant is The Kendall Company, L.P.. The 510(k) number is K990530.

When did KERLIX MD ANTIMICROBIAL GAUZE DRESSING receive FDA 510(k) clearance?

KERLIX MD ANTIMICROBIAL GAUZE DRESSING received FDA 510(k) clearance on 2000-01-31, under 510(k) number K990530.

Who is the listed applicant for KERLIX MD ANTIMICROBIAL GAUZE DRESSING?

The FDA 510(k) record lists The Kendall Company, L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KERLIX MD ANTIMICROBIAL GAUZE DRESSING?

The FDA product code for KERLIX MD ANTIMICROBIAL GAUZE DRESSING is NAD.

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Other records listing The Kendall Company, L.P. as applicant

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Related Devices (Code: NAD)

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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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