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FDA 510(k)

MAGNETIC DRAPE - INSTRUMENT HOLDER

K-Number: K780865 · 1978-08-21

ApplicantDevon Industries, Inc.
Decision Date1978-08-21
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MAGNETIC DRAPE - INSTRUMENT HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Devon Industries, Inc.. It received FDA 510(k) clearance on 1978-08-21 under 510(k) number K780865. 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 MAGNETIC DRAPE - INSTRUMENT HOLDER?

MAGNETIC DRAPE - INSTRUMENT HOLDER is a medical device that received FDA 510(k) clearance on 1978-08-21. The listed applicant is Devon Industries, Inc.. The 510(k) number is K780865.

When did MAGNETIC DRAPE - INSTRUMENT HOLDER receive FDA 510(k) clearance?

MAGNETIC DRAPE - INSTRUMENT HOLDER received FDA 510(k) clearance on 1978-08-21, under 510(k) number K780865.

Who is the listed applicant for MAGNETIC DRAPE - INSTRUMENT HOLDER?

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

What is the FDA product code for MAGNETIC DRAPE - INSTRUMENT HOLDER?

The FDA product code for MAGNETIC DRAPE - INSTRUMENT HOLDER is KKX.

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Other records listing Devon Industries, 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.

K961993BIRTHDAY KIT (OBSTETRICAL DELIVERY KIT)K954015ABG POINT LOK NEEDLE PROTECTION DEVICEK946289DEVONS POINT LOK NEEDLE PROTECTION DEVICEK944114PHLEBOTOMY UNIT SHARPS A GATORK943892POINT OF USE SHARPS A GATORK945197THE SHARPS COLLECTION AND DISPOSAL SYSTEM

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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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