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)

TRIMAX RADIOGRAPHIC CASSETTE

K-Number: K980722 · 1998-03-23

ApplicantImation Corp.
Decision Date1998-03-23
Product CodeIXA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TRIMAX RADIOGRAPHIC CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Imation Corp.. It received FDA 510(k) clearance on 1998-03-23 under 510(k) number K980722. The device is classified under product code IXA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIMAX RADIOGRAPHIC CASSETTE?

TRIMAX RADIOGRAPHIC CASSETTE is a medical device that received FDA 510(k) clearance on 1998-03-23. The listed applicant is Imation Corp.. The 510(k) number is K980722.

When did TRIMAX RADIOGRAPHIC CASSETTE receive FDA 510(k) clearance?

TRIMAX RADIOGRAPHIC CASSETTE received FDA 510(k) clearance on 1998-03-23, under 510(k) number K980722.

Who is the listed applicant for TRIMAX RADIOGRAPHIC CASSETTE?

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

What is the FDA product code for TRIMAX RADIOGRAPHIC CASSETTE?

The FDA product code for TRIMAX RADIOGRAPHIC CASSETTE is IXA.

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 Imation 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.

K984252IMATION TRIMATIC DIGITAL SYSTEMK973303IMATION MODEL 9410 NETWORK INTERFACEK972163IMATION SE-196 LASER IMAGERK9627503M TRIMATIC MODULAR ADVANCED PROCESSING SYSTEM AND 3M APS AUTOMATIC FILM PROCESSOR

Related Devices (Code: IXA)

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.

K081557PORTABLE SUPINE PATIENT SUPPORT AND CASSETTE HOLDERJddb Manufacturing, Inc.K053173DS CASSETTEKonica Minolta Medical & Graphic, Inc.K040378KODAK DIRECTVIEW CR CASSETTE/GP/15 X 30 CM, CATALOG# 8418253Eastman Kodak CompanyK023020AGFA MAMORAY MAMMOGRAPHIC CASSETTE, AGFA METAL-BODIED CAWO CASSETTE, AGFA CURIX AND LIGHTWEIGHT CASSETTEAgfa Corp.K021903KODAK X-OMAT CASSETTE/LEADLESS FOR DENTAL USEEastman Kodak CompanyK013686KODAK DIRECTVIEW TABLETOP CASSETTEEastman 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.

↑