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FDA 510(k)

AP-6CR CINERADIOGRAPHIC FILM PROCESSOR

K-Number: K915365 · 1992-08-27

ApplicantThe Allen Products Co.
Decision Date1992-08-27
Product CodeIXX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AP-6CR CINERADIOGRAPHIC FILM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is The Allen Products Co.. It received FDA 510(k) clearance on 1992-08-27 under 510(k) number K915365. The device is classified under product code IXX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AP-6CR CINERADIOGRAPHIC FILM PROCESSOR?

AP-6CR CINERADIOGRAPHIC FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 1992-08-27. The listed applicant is The Allen Products Co.. The 510(k) number is K915365.

When did AP-6CR CINERADIOGRAPHIC FILM PROCESSOR receive FDA 510(k) clearance?

AP-6CR CINERADIOGRAPHIC FILM PROCESSOR received FDA 510(k) clearance on 1992-08-27, under 510(k) number K915365.

Who is the listed applicant for AP-6CR CINERADIOGRAPHIC FILM PROCESSOR?

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

What is the FDA product code for AP-6CR CINERADIOGRAPHIC FILM PROCESSOR?

The FDA product code for AP-6CR CINERADIOGRAPHIC FILM PROCESSOR is IXX.

Related Clinical Trials

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.

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Other records listing The Allen Products Co. 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.

K850421CINE RADIOGRAPHIC FILM PROCESSOR M-45CRK841431RADIOGRAPHIC FILM PROCESSOR M-30CR &

Related Devices (Code: IXX)

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.

K963334JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100Jamieson Film Co.K913241JAMIESON JT-CRP CINE FILM PROCESSORJamieson Film Co.K861928STERILE O. R. TOWELAnago, Inc.K850421CINE RADIOGRAPHIC FILM PROCESSOR M-45CRThe Allen Products Co.K841431RADIOGRAPHIC FILM PROCESSOR M-30CR &The Allen Products Co.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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