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FDA 510(k)

HUESTIS FLEXI-HOLDER

K-Number: K792721 · 1980-02-19

ApplicantHuestis Machine Corp.
Decision Date1980-02-19
Product CodeIXA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HUESTIS FLEXI-HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Huestis Machine Corp.. It received FDA 510(k) clearance on 1980-02-19 under 510(k) number K792721. The device is classified under product code IXA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUESTIS FLEXI-HOLDER?

HUESTIS FLEXI-HOLDER is a medical device that received FDA 510(k) clearance on 1980-02-19. The listed applicant is Huestis Machine Corp.. The 510(k) number is K792721.

When did HUESTIS FLEXI-HOLDER receive FDA 510(k) clearance?

HUESTIS FLEXI-HOLDER received FDA 510(k) clearance on 1980-02-19, under 510(k) number K792721.

Who is the listed applicant for HUESTIS FLEXI-HOLDER?

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

What is the FDA product code for HUESTIS FLEXI-HOLDER?

The FDA product code for HUESTIS FLEXI-HOLDER is IXA.

Related Clinical Trials

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Other records listing Huestis Machine 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.

K940145COMPU-CUTTER THERAPEUTIC SHIELDING CUTTING DEVICEK926187POSICAST IMMOBILIZATION SYSTEMK904005HUESTIS FLEXI-BOARDK901567THE HUESTIS COMPU-PLOTTERK880047HUESTIS COMPU-FORMER

Related Devices (Code: IXA)

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.

K081557PORTABLE SUPINE PATIENT SUPPORT AND CASSETTE HOLDERJddb Manufacturing, Inc.K053173DS CASSETTEKonica Minolta Medical & Graphic, Inc.K040378KODAK DIRECTVIEW CR CASSETTE/GP/15 X 30 CM, CATALOG# 8418253Eastman Kodak CompanyK023020AGFA MAMORAY MAMMOGRAPHIC CASSETTE, AGFA METAL-BODIED CAWO CASSETTE, AGFA CURIX AND LIGHTWEIGHT CASSETTEAgfa Corp.K021903KODAK X-OMAT CASSETTE/LEADLESS FOR DENTAL USEEastman Kodak CompanyK013686KODAK DIRECTVIEW TABLETOP CASSETTEEastman Kodak Company

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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