FDA 510(k)

CRONEX LOW ABSORPTION CASSETTE

K-Number: K952891 · 1995-07-13

Decision Date1995-07-13

Product CodeIXA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CRONEX LOW ABSORPTION CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is The DU Pont Co.. It received FDA 510(k) clearance on 1995-07-13 under 510(k) number K952891. 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 LOW ABSORPTION CASSETTE?

CRONEX LOW ABSORPTION CASSETTE is a medical device that received FDA 510(k) clearance on 1995-07-13. The listed applicant is The DU Pont Co.. The 510(k) number is K952891.

When did CRONEX LOW ABSORPTION CASSETTE receive FDA 510(k) clearance?

CRONEX LOW ABSORPTION CASSETTE received FDA 510(k) clearance on 1995-07-13, under 510(k) number K952891.

Who is the listed applicant for CRONEX LOW ABSORPTION CASSETTE?

The FDA 510(k) record lists The DU Pont Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CRONEX LOW ABSORPTION CASSETTE?

The FDA product code for CRONEX LOW ABSORPTION CASSETTE is IXA.

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Other records listing The DU Pont Co. as applicant

K953477MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING K953475CDS COMPACT DAYLIGHT CASSETTE FOR VIDEO IMAGING K945125DUPONT ACA VANCOMYCIN (VANC) METHOD K943704LIPASE CALIBRATOR K900492LABELING CHANGE - VIASPAN(TM) (BELZER UW)K885259ACA THYRONINE UPTAKE (TU E) METHOD

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Related Devices (Code: IXA)

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 Company K023020AGFA MAMORAY MAMMOGRAPHIC CASSETTE, AGFA METAL-BODIED CAWO CASSETTE, AGFA CURIX AND LIGHTWEIGHT CASSETTEAgfa Corp.K021903KODAK X-OMAT CASSETTE/LEADLESS FOR DENTAL USEEastman Kodak Company K013686KODAK 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.