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FDA 510(k)

HVO, INC., DISPOSABLE NON-STERILE SURGICAL DRAPES

K-Number: K050508 · 2005-04-27

ApplicantHaywood Vocational Opportunities
Decision Date2005-04-27
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HVO, INC., DISPOSABLE NON-STERILE SURGICAL DRAPES is the device name listed in this FDA 510(k) record. The listed applicant is Haywood Vocational Opportunities. It received FDA 510(k) clearance on 2005-04-27 under 510(k) number K050508. 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 HVO, INC., DISPOSABLE NON-STERILE SURGICAL DRAPES?

HVO, INC., DISPOSABLE NON-STERILE SURGICAL DRAPES is a medical device that received FDA 510(k) clearance on 2005-04-27. The listed applicant is Haywood Vocational Opportunities. The 510(k) number is K050508.

When did HVO, INC., DISPOSABLE NON-STERILE SURGICAL DRAPES receive FDA 510(k) clearance?

HVO, INC., DISPOSABLE NON-STERILE SURGICAL DRAPES received FDA 510(k) clearance on 2005-04-27, under 510(k) number K050508.

Who is the listed applicant for HVO, INC., DISPOSABLE NON-STERILE SURGICAL DRAPES?

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

What is the FDA product code for HVO, INC., DISPOSABLE NON-STERILE SURGICAL DRAPES?

The FDA product code for HVO, INC., DISPOSABLE NON-STERILE SURGICAL DRAPES is KKX.

Related Clinical Trials

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Other records listing Haywood Vocational Opportunities 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.

K023005AQUILLA MODULAR WHEELCHAIR

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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