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FDA 510(k)

KODAK DIGITAL SCIENCE REMOTE CASSETTE

K-Number: K962896 · 1996-09-20

ApplicantEastman Kodak Company
Decision Date1996-09-20
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK DIGITAL SCIENCE REMOTE CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Eastman Kodak Company. It received FDA 510(k) clearance on 1996-09-20 under 510(k) number K962896. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK DIGITAL SCIENCE REMOTE CASSETTE?

KODAK DIGITAL SCIENCE REMOTE CASSETTE is a medical device that received FDA 510(k) clearance on 1996-09-20. The listed applicant is Eastman Kodak Company. The 510(k) number is K962896.

When did KODAK DIGITAL SCIENCE REMOTE CASSETTE receive FDA 510(k) clearance?

KODAK DIGITAL SCIENCE REMOTE CASSETTE received FDA 510(k) clearance on 1996-09-20, under 510(k) number K962896.

Who is the listed applicant for KODAK DIGITAL SCIENCE REMOTE CASSETTE?

The FDA 510(k) record lists Eastman Kodak Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KODAK DIGITAL SCIENCE REMOTE CASSETTE?

The FDA product code for KODAK DIGITAL SCIENCE REMOTE CASSETTE is KPR.

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Other records listing Eastman Kodak Company 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.

K060550KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386K060137KODAK ECLIPSE IMAGE PROCESSING SOFTWAREK060079KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEMK060055KODAK PACSK053347KODAK CARESTREAM PACSK051483KODAK DIRECTVIEW DR SYSTEM DETECTOR

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Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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