BETHEL PLUS MULTIPLE NAMES— 510(k) K912042

Name: FDA 510(k) clearance K912042
Creator: U.S. Food and Drug Administration
Published: 1991-07-02

Substantially Equivalent

Bethel Latex Products, Inc.

FDA 510(k) clearance K912042 for BETHEL PLUS MULTIPLE NAMES, Substantially Equivalent on 1991-07-02. Applicant: Bethel Latex Products, Inc.. Device class: 1.

Clearance details

Applicant: Bethel Latex Products, Inc.
Product code: Code LZB
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1991-05-08
Decision date: 1991-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Haz;Ejirst, MS, US

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