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FDA 510(k)

JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100

K-Number: K963334 · 1996-09-11

ApplicantJamieson Film Co.
Decision Date1996-09-11
Product CodeIXX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100 is the device name listed in this FDA 510(k) record. The listed applicant is Jamieson Film Co.. It received FDA 510(k) clearance on 1996-09-11 under 510(k) number K963334. 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 JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100?

JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100 is a medical device that received FDA 510(k) clearance on 1996-09-11. The listed applicant is Jamieson Film Co.. The 510(k) number is K963334.

When did JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100 receive FDA 510(k) clearance?

JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100 received FDA 510(k) clearance on 1996-09-11, under 510(k) number K963334.

Who is the listed applicant for JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100?

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

What is the FDA product code for JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100?

The FDA product code for JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Jamieson Film 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.

K970738KODAK DIGITAL SCIENCE CARDIAC DIGITAL ACQUISITION UNITK971128CAP-35B III/CINE 275K960043KODAK CARDIOLOGY DIGITAL ARCHIVE & REVIEW SYSTEMK953563VANGUARD XR-350 CINEANGIOGRAM PROJECTORK913241JAMIESON JT-CRP CINE FILM PROCESSOR

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.

K915365AP-6CR CINERADIOGRAPHIC FILM PROCESSORThe Allen Products 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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