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FDA 510(k)

CONVERTORS EQUIPMENT DRAPES

K-Number: K000417 · 2000-03-17

ApplicantAllegiance Healthcare Corp.
Decision Date2000-03-17
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONVERTORS EQUIPMENT DRAPES is the device name listed in this FDA 510(k) record. The listed applicant is Allegiance Healthcare Corp.. It received FDA 510(k) clearance on 2000-03-17 under 510(k) number K000417. 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 CONVERTORS EQUIPMENT DRAPES?

CONVERTORS EQUIPMENT DRAPES is a medical device that received FDA 510(k) clearance on 2000-03-17. The listed applicant is Allegiance Healthcare Corp.. The 510(k) number is K000417.

When did CONVERTORS EQUIPMENT DRAPES receive FDA 510(k) clearance?

CONVERTORS EQUIPMENT DRAPES received FDA 510(k) clearance on 2000-03-17, under 510(k) number K000417.

Who is the listed applicant for CONVERTORS EQUIPMENT DRAPES?

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

What is the FDA product code for CONVERTORS EQUIPMENT DRAPES?

The FDA product code for CONVERTORS EQUIPMENT DRAPES is KKX.

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Other records listing Allegiance Healthcare Corp. 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.

K023673AIRLIFE DEMAND NASAL CANNULAK023419TRILAMINATE DRAPES/TIBURONK024120MODIFICATION TO TEMNO BIOPSY NEEDLESK024292MODIFICATION TO POSITIVE TOUCH POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN AND CHEMOTHERAPY LABELING CLAIMK024102DENTAL POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIMK023425DRAPES WITH ABSORBENT REINFORCEMENT

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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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