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FDA 510(k)

BUSSE SURGICAL DRAPE

K-Number: K083424 · 2009-02-26

ApplicantBusse Hosipital Disposables
Decision Date2009-02-26
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BUSSE SURGICAL DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Busse Hosipital Disposables. It received FDA 510(k) clearance on 2009-02-26 under 510(k) number K083424. 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 BUSSE SURGICAL DRAPE?

BUSSE SURGICAL DRAPE is a medical device that received FDA 510(k) clearance on 2009-02-26. The listed applicant is Busse Hosipital Disposables. The 510(k) number is K083424.

When did BUSSE SURGICAL DRAPE receive FDA 510(k) clearance?

BUSSE SURGICAL DRAPE received FDA 510(k) clearance on 2009-02-26, under 510(k) number K083424.

Who is the listed applicant for BUSSE SURGICAL DRAPE?

The FDA 510(k) record lists Busse Hosipital Disposables as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUSSE SURGICAL DRAPE?

The FDA product code for BUSSE SURGICAL DRAPE is KKX.

Related Clinical Trials

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.

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Other records listing Busse Hosipital Disposables as applicant

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.

K080804BUSSE PLASTIC LOR SYRINGE

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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