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FDA 510(k)

MASTER & FRANK SURGICAL DRAPES (STERILE)

K-Number: K020393 · 2002-05-03

ApplicantMaster & Frank Enterprses Co., Ltd.
Decision Date2002-05-03
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MASTER & FRANK SURGICAL DRAPES (STERILE) is the device name listed in this FDA 510(k) record. The listed applicant is Master & Frank Enterprses Co., Ltd.. It received FDA 510(k) clearance on 2002-05-03 under 510(k) number K020393. 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 MASTER & FRANK SURGICAL DRAPES (STERILE)?

MASTER & FRANK SURGICAL DRAPES (STERILE) is a medical device that received FDA 510(k) clearance on 2002-05-03. The listed applicant is Master & Frank Enterprses Co., Ltd.. The 510(k) number is K020393.

When did MASTER & FRANK SURGICAL DRAPES (STERILE) receive FDA 510(k) clearance?

MASTER & FRANK SURGICAL DRAPES (STERILE) received FDA 510(k) clearance on 2002-05-03, under 510(k) number K020393.

Who is the listed applicant for MASTER & FRANK SURGICAL DRAPES (STERILE)?

The FDA 510(k) record lists Master & Frank Enterprses Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASTER & FRANK SURGICAL DRAPES (STERILE)?

The FDA product code for MASTER & FRANK SURGICAL DRAPES (STERILE) is KKX.

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Related Devices (Code: KKX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K230645BeneHold™ Surgical Incise Drape with CHG antimicrobial IIAvery Dennison Medical , Ltd.K2225783M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)3M CompanyK202208BeneHold Surgical Incise Drape with CHG antimicrobialAvery Dennison Belgie BvbaK200238ControlRad Sterile CoverControlrad, Inc.K163556MediClear PreOpCovalontechnologies, Inc.K130404TIBURON SURGICAL DRAPECardinal Health200, LLC

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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