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FDA 510(k)

STERILE DISPOSABLE EQUIPMENT MAGNET COVER

K-Number: K970185 · 1997-04-10

ApplicantContour Fabricators, Inc.
Decision Date1997-04-10
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE DISPOSABLE EQUIPMENT MAGNET COVER is the device name listed in this FDA 510(k) record. The listed applicant is Contour Fabricators, Inc.. It received FDA 510(k) clearance on 1997-04-10 under 510(k) number K970185. 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 STERILE DISPOSABLE EQUIPMENT MAGNET COVER?

STERILE DISPOSABLE EQUIPMENT MAGNET COVER is a medical device that received FDA 510(k) clearance on 1997-04-10. The listed applicant is Contour Fabricators, Inc.. The 510(k) number is K970185.

When did STERILE DISPOSABLE EQUIPMENT MAGNET COVER receive FDA 510(k) clearance?

STERILE DISPOSABLE EQUIPMENT MAGNET COVER received FDA 510(k) clearance on 1997-04-10, under 510(k) number K970185.

Who is the listed applicant for STERILE DISPOSABLE EQUIPMENT MAGNET COVER?

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

What is the FDA product code for STERILE DISPOSABLE EQUIPMENT MAGNET COVER?

The FDA product code for STERILE DISPOSABLE EQUIPMENT MAGNET COVER is KKX.

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Other records listing Contour Fabricators, 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.

K090773CFI ULTRASOUND PROBE DRAPEK970900INSTRUMENT HOLDERK971040CABLE HOLDER, SUCTION TUBE HOLDERK964141GE STERILE DISPOSABLE EQUIPMENT COIL COVERK963453CFI RESTRAINT BELT (CFI-168) / CFI RESTRAINT BELT (CFI-4046)K820692BANDBAG, WRAP, STERILE

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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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