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FDA 510(k)

MEDLINE ASEP PLUS SURGICAL DRAPES

K-Number: K023432 · 2002-11-04

ApplicantMedline Industries, Inc.
Decision Date2002-11-04
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDLINE ASEP PLUS SURGICAL DRAPES 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 2002-11-04 under 510(k) number K023432. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE ASEP PLUS SURGICAL DRAPES?

MEDLINE ASEP PLUS SURGICAL DRAPES is a medical device that received FDA 510(k) clearance on 2002-11-04. The listed applicant is Medline Industries, Inc.. The 510(k) number is K023432.

When did MEDLINE ASEP PLUS SURGICAL DRAPES receive FDA 510(k) clearance?

MEDLINE ASEP PLUS SURGICAL DRAPES received FDA 510(k) clearance on 2002-11-04, under 510(k) number K023432.

Who is the listed applicant for MEDLINE ASEP PLUS SURGICAL DRAPES?

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 ASEP PLUS SURGICAL DRAPES?

The FDA product code for MEDLINE ASEP PLUS SURGICAL DRAPES is KKX.

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Related Devices (Code: KKX)

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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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