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FDA 510(k)

DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE

K-Number: K880513 · 1988-03-11

ApplicantTaub Industries
Decision Date1988-03-11
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Taub Industries. It received FDA 510(k) clearance on 1988-03-11 under 510(k) number K880513. 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 DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE?

DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE is a medical device that received FDA 510(k) clearance on 1988-03-11. The listed applicant is Taub Industries. The 510(k) number is K880513.

When did DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE receive FDA 510(k) clearance?

DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE received FDA 510(k) clearance on 1988-03-11, under 510(k) number K880513.

Who is the listed applicant for DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE?

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

What is the FDA product code for DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE?

The FDA product code for DISP. NON-MAGNETIC SURGICAL INSTRU. 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 Taub Industries 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.

K822847INSTA-HOLD

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

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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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