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)

KENEX MOBILE CASSETT HOLDER (AS EXHIBIT #7)

K-Number: K951006 · 1995-04-03

ApplicantKenex , Ltd.
Decision Date1995-04-03
Product CodeIXA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KENEX MOBILE CASSETT HOLDER (AS EXHIBIT #7) is the device name listed in this FDA 510(k) record. The listed applicant is Kenex , Ltd.. It received FDA 510(k) clearance on 1995-04-03 under 510(k) number K951006. 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 KENEX MOBILE CASSETT HOLDER (AS EXHIBIT #7)?

KENEX MOBILE CASSETT HOLDER (AS EXHIBIT #7) is a medical device that received FDA 510(k) clearance on 1995-04-03. The listed applicant is Kenex , Ltd.. The 510(k) number is K951006.

When did KENEX MOBILE CASSETT HOLDER (AS EXHIBIT #7) receive FDA 510(k) clearance?

KENEX MOBILE CASSETT HOLDER (AS EXHIBIT #7) received FDA 510(k) clearance on 1995-04-03, under 510(k) number K951006.

Who is the listed applicant for KENEX MOBILE CASSETT HOLDER (AS EXHIBIT #7)?

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

What is the FDA product code for KENEX MOBILE CASSETT HOLDER (AS EXHIBIT #7)?

The FDA product code for KENEX MOBILE CASSETT HOLDER (AS EXHIBIT #7) 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 Kenex , Ltd. 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.

K951005KENEX INJECTOR HEAD SUPPORT (AS EXHIBIT 2)K9510042001 SPECIAL PROCEDURE LAMP (LOW VOLTAGE) (AS EXHIBITS #2 & 4)K951003KENEX RADIATION SHIELD (VARIOUS MODELS AS EXHIBITS #2 & 5)

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.

↑