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FDA 510(k)

CRONEX RADIATION THERAPY VERIFICATION CASSETTE

K-Number: K953725 · 1995-09-06

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1995-09-06
Product CodeIXA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CRONEX RADIATION THERAPY VERIFICATION CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1995-09-06 under 510(k) number K953725. 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 CRONEX RADIATION THERAPY VERIFICATION CASSETTE?

CRONEX RADIATION THERAPY VERIFICATION CASSETTE is a medical device that received FDA 510(k) clearance on 1995-09-06. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K953725.

When did CRONEX RADIATION THERAPY VERIFICATION CASSETTE receive FDA 510(k) clearance?

CRONEX RADIATION THERAPY VERIFICATION CASSETTE received FDA 510(k) clearance on 1995-09-06, under 510(k) number K953725.

Who is the listed applicant for CRONEX RADIATION THERAPY VERIFICATION CASSETTE?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRONEX RADIATION THERAPY VERIFICATION CASSETTE?

The FDA product code for CRONEX RADIATION THERAPY VERIFICATION CASSETTE is IXA.

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Other records listing E.I. Dupont DE Nemours & Co., 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.

K951851ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAYK953724CRONEX RADIATION THERAPY CASSETTEK951441DUPONT ACA DIGOXIN (DGN A) METHODK950137URINE BARBITURATES SCREEN FLEX(TM) REAGENT CARTRIDGEK950136URINE OPIATES SCREEN FLEX(TM) REAGENT CARTRIDGEK950181URINE CANNABINOIDS SCREEN FLEX(TM) REAGENT CARTRIDGE

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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

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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