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FDA 510(k)

CM & CM DS-7

K-Number: K963914 · 1997-10-08

ApplicantKonica Medical Corp.
Decision Date1997-10-08
Product CodeIXA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CM & CM DS-7 is the device name listed in this FDA 510(k) record. The listed applicant is Konica Medical Corp.. It received FDA 510(k) clearance on 1997-10-08 under 510(k) number K963914. 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 CM & CM DS-7?

CM & CM DS-7 is a medical device that received FDA 510(k) clearance on 1997-10-08. The listed applicant is Konica Medical Corp.. The 510(k) number is K963914.

When did CM & CM DS-7 receive FDA 510(k) clearance?

CM & CM DS-7 received FDA 510(k) clearance on 1997-10-08, under 510(k) number K963914.

Who is the listed applicant for CM & CM DS-7?

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

What is the FDA product code for CM & CM DS-7?

The FDA product code for CM & CM DS-7 is IXA.

Other records listing Konica Medical 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.

K990969KONICA SRX- 701 AUTOMATIC X-RAY FILM PROCESSORK963913MD100 & MM150K955583VIFSK931316KONICA DS-7 AUTOMATIC X-RAY FILM PROCESSORK933830KONICA LD-4500 LASER DIGITIZERK931317KONICA SRX-301 AUTOMATIC X-RAY FILM PROCESSOR

View all 12 devices →

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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