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FDA 510(k)

3M X-LARGE SHEET #7979/ #7979NS

K-Number: K946025 · 1995-02-02

Applicant3M Healthcare
Decision Date1995-02-02
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

3M X-LARGE SHEET #7979/ #7979NS is the device name listed in this FDA 510(k) record. The listed applicant is 3M Healthcare. It received FDA 510(k) clearance on 1995-02-02 under 510(k) number K946025. 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 3M X-LARGE SHEET #7979/ #7979NS?

3M X-LARGE SHEET #7979/ #7979NS is a medical device that received FDA 510(k) clearance on 1995-02-02. The listed applicant is 3M Healthcare. The 510(k) number is K946025.

When did 3M X-LARGE SHEET #7979/ #7979NS receive FDA 510(k) clearance?

3M X-LARGE SHEET #7979/ #7979NS received FDA 510(k) clearance on 1995-02-02, under 510(k) number K946025.

Who is the listed applicant for 3M X-LARGE SHEET #7979/ #7979NS?

The FDA 510(k) record lists 3M Healthcare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3M X-LARGE SHEET #7979/ #7979NS?

The FDA product code for 3M X-LARGE SHEET #7979/ #7979NS is KKX.

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Related Devices (Code: KKX)

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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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