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FDA 510(k)

UNIVERSAL VIDEO/LASER ARM DRAPE

K-Number: K934630 · 1994-10-28

ApplicantHydro-Med Products, Inc.
Decision Date1994-10-28
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL VIDEO/LASER ARM DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Hydro-Med Products, Inc.. It received FDA 510(k) clearance on 1994-10-28 under 510(k) number K934630. 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 UNIVERSAL VIDEO/LASER ARM DRAPE?

UNIVERSAL VIDEO/LASER ARM DRAPE is a medical device that received FDA 510(k) clearance on 1994-10-28. The listed applicant is Hydro-Med Products, Inc.. The 510(k) number is K934630.

When did UNIVERSAL VIDEO/LASER ARM DRAPE receive FDA 510(k) clearance?

UNIVERSAL VIDEO/LASER ARM DRAPE received FDA 510(k) clearance on 1994-10-28, under 510(k) number K934630.

Who is the listed applicant for UNIVERSAL VIDEO/LASER ARM DRAPE?

The FDA 510(k) record lists Hydro-Med Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIVERSAL VIDEO/LASER ARM DRAPE?

The FDA product code for UNIVERSAL VIDEO/LASER ARM DRAPE is KKX.

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Other records listing Hydro-Med Products, Inc. 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.

K944198SURGICAL MICROSCOPE DRAPEK940151ULTRASOUND PROBE DRAPEK940152CAMERA COVER WITH TEAR TIPK923099X-RAY DRAPESK863872TAMPER HAMPERK853281EASYTOP

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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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