Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CINE RADIOGRAPHIC FILM PROCESSOR M-45CR

K-Number: K850421 · 1985-03-22

ApplicantThe Allen Products Co.
Decision Date1985-03-22
Product CodeIXX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CINE RADIOGRAPHIC FILM PROCESSOR M-45CR 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 1985-03-22 under 510(k) number K850421. 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 CINE RADIOGRAPHIC FILM PROCESSOR M-45CR?

CINE RADIOGRAPHIC FILM PROCESSOR M-45CR is a medical device that received FDA 510(k) clearance on 1985-03-22. The listed applicant is The Allen Products Co.. The 510(k) number is K850421.

When did CINE RADIOGRAPHIC FILM PROCESSOR M-45CR receive FDA 510(k) clearance?

CINE RADIOGRAPHIC FILM PROCESSOR M-45CR received FDA 510(k) clearance on 1985-03-22, under 510(k) number K850421.

Who is the listed applicant for CINE RADIOGRAPHIC FILM PROCESSOR M-45CR?

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 CINE RADIOGRAPHIC FILM PROCESSOR M-45CR?

The FDA product code for CINE RADIOGRAPHIC FILM PROCESSOR M-45CR 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 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.

K915365AP-6CR CINERADIOGRAPHIC FILM PROCESSORK841431RADIOGRAPHIC 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.K915365AP-6CR CINERADIOGRAPHIC FILM PROCESSORThe Allen Products Co.K913241JAMIESON JT-CRP CINE FILM PROCESSORJamieson Film Co.K861928STERILE O. R. TOWELAnago, Inc.K841431RADIOGRAPHIC FILM PROCESSOR M-30CR &The Allen Products Co.

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.

↑