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FDA 510(k)

POLAROID RADIOGRAPHIC FILM PROCESSOR

K-Number: K812088 · 1981-08-31

ApplicantPolaroid Corp.
Decision Date1981-08-31
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POLAROID RADIOGRAPHIC FILM PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Polaroid Corp.. It received FDA 510(k) clearance on 1981-08-31 under 510(k) number K812088. 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 POLAROID RADIOGRAPHIC FILM PROCESSOR?

POLAROID RADIOGRAPHIC FILM PROCESSOR is a medical device that received FDA 510(k) clearance on 1981-08-31. The listed applicant is Polaroid Corp.. The 510(k) number is K812088.

When did POLAROID RADIOGRAPHIC FILM PROCESSOR receive FDA 510(k) clearance?

POLAROID RADIOGRAPHIC FILM PROCESSOR received FDA 510(k) clearance on 1981-08-31, under 510(k) number K812088.

Who is the listed applicant for POLAROID RADIOGRAPHIC FILM PROCESSOR?

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

What is the FDA product code for POLAROID RADIOGRAPHIC FILM PROCESSOR?

The FDA product code for POLAROID RADIOGRAPHIC FILM PROCESSOR is IXW.

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 Polaroid 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.

K812542POLAROID INSTANT ENDOCAMERAK812089POLAROID RADIOGRAPHIC FILM CASSETTEK811352POLAROID TPX RADIOGRAPHIC FILMK792512POLAROID LAND CAMERA FOR ENDOSCOPY

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

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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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