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FDA 510(k)

KODAK REMOTE ALARM UNIT

K-Number: K874926 · 1988-01-04

ApplicantEastman Kodak Company
Decision Date1988-01-04
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK REMOTE ALARM UNIT 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 1988-01-04 under 510(k) number K874926. The device is classified under product code IXW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK REMOTE ALARM UNIT?

KODAK REMOTE ALARM UNIT is a medical device that received FDA 510(k) clearance on 1988-01-04. The listed applicant is Eastman Kodak Company. The 510(k) number is K874926.

When did KODAK REMOTE ALARM UNIT receive FDA 510(k) clearance?

KODAK REMOTE ALARM UNIT received FDA 510(k) clearance on 1988-01-04, under 510(k) number K874926.

Who is the listed applicant for KODAK REMOTE ALARM UNIT?

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 REMOTE ALARM UNIT?

The FDA product code for KODAK REMOTE ALARM UNIT is IXW.

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Other records listing Eastman Kodak Company as applicant

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Related Devices (Code: IXW)

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.

K111167XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINTVelopex International, Inc.K093503INTRAX FILM PROCESSORVelopex International, Inc.K091628OPTIMAX, COMPACT 2, OPTIMAX 2010, ECOMAXProtec GmbH & Co. KGK024342RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000Daito Co., Ltd.K023801FILM PROCESSOR, MODEL LIFE RAY PRO 1000S.A.I.E.P. S.R.L.K023825FILM PROCESSOR, MODEL LIFE RAY PRO 2500S.A.I.E.P. S.R.L.

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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