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)

POLAROID TPX RADIOGRAPHIC FILM

K-Number: K811352 · 1981-06-18

ApplicantPolaroid Corp.
Decision Date1981-06-18
Product CodeIWZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POLAROID TPX RADIOGRAPHIC FILM is the device name listed in this FDA 510(k) record. The listed applicant is Polaroid Corp.. It received FDA 510(k) clearance on 1981-06-18 under 510(k) number K811352. The device is classified under product code IWZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLAROID TPX RADIOGRAPHIC FILM?

POLAROID TPX RADIOGRAPHIC FILM is a medical device that received FDA 510(k) clearance on 1981-06-18. The listed applicant is Polaroid Corp.. The 510(k) number is K811352.

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

POLAROID TPX RADIOGRAPHIC FILM received FDA 510(k) clearance on 1981-06-18, under 510(k) number K811352.

Who is the listed applicant for POLAROID TPX RADIOGRAPHIC FILM?

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 TPX RADIOGRAPHIC FILM?

The FDA product code for POLAROID TPX RADIOGRAPHIC FILM is IWZ.

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 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 CASSETTEK812088POLAROID RADIOGRAPHIC FILM PROCESSORK792512POLAROID LAND CAMERA FOR ENDOSCOPY

Related Devices (Code: IWZ)

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.

K970154KODAK EKTASIAN HG FILM (EHG-15)Eastman Kodak CompanyK954200VOXGRAMVoxelK9316043M MEDICAL DIAGNOSTIC VIDEOCASSETTE3M Health Care, Ltd.K9316053M MEDICAL DIAGNOSTIC SUPER VHS VIDEOCASSETTE3M Health Care, Ltd.K920539ORWO X-RAY FILMBurkhart Roentgen Intl., Inc.K884827KODAK DENTAL BARRIER PACEastman Kodak Company

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.

↑