KENEX MOBILE CASSETT HOLDER (AS EXHIBIT #7)— 510(k) K951006

Name: FDA 510(k) clearance K951006
Creator: U.S. Food and Drug Administration
Published: 1995-04-03

Substantially Equivalent

Kenex , Ltd.

FDA 510(k) clearance K951006 for KENEX MOBILE CASSETT HOLDER (AS EXHIBIT #7), Substantially Equivalent on 1995-04-03. Applicant: Kenex , Ltd.. Device class: 2.

Clearance details

Applicant: Kenex , Ltd.
Product code: Code IXA
Device class: Class 2
Regulation: 21 CFR 892.1850
Advisory panel: Radiology
Date received: 1995-02-15
Decision date: 1995-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: England, GB

Download summary PDF View on FDA.gov ↗

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K951005 — KENEX INJECTOR HEAD SUPPORT (AS EXHIBIT 2)1995-05-04
K951004 — 2001 SPECIAL PROCEDURE LAMP (LOW VOLTAGE) (AS EXHIBITS #2 & 4)1995-04-10
K951003 — KENEX RADIATION SHIELD (VARIOUS MODELS AS EXHIBITS #2 & 5)1995-04-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.