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FDA 510(k)

RADIOGRAPHIC FILM CASSETTES

K-Number: K962336 · 1996-07-03

ApplicantUnidex Group, Inc.
Decision Date1996-07-03
Product CodeIXA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIOGRAPHIC FILM CASSETTES is the device name listed in this FDA 510(k) record. The listed applicant is Unidex Group, Inc.. It received FDA 510(k) clearance on 1996-07-03 under 510(k) number K962336. 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 RADIOGRAPHIC FILM CASSETTES?

RADIOGRAPHIC FILM CASSETTES is a medical device that received FDA 510(k) clearance on 1996-07-03. The listed applicant is Unidex Group, Inc.. The 510(k) number is K962336.

When did RADIOGRAPHIC FILM CASSETTES receive FDA 510(k) clearance?

RADIOGRAPHIC FILM CASSETTES received FDA 510(k) clearance on 1996-07-03, under 510(k) number K962336.

Who is the listed applicant for RADIOGRAPHIC FILM CASSETTES?

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

What is the FDA product code for RADIOGRAPHIC FILM CASSETTES?

The FDA product code for RADIOGRAPHIC FILM CASSETTES is IXA.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Unidex Group, 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.

K962338RADIOGRAPHIC GRID

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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