MBI FIBEROPTIC ENDO-ILLUMINATOR— 510(k) K961036

Name: FDA 510(k) clearance K961036
Creator: U.S. Food and Drug Administration
Published: 1996-07-15

Substantially Equivalent

M.B. Industries, Inc.

FDA 510(k) clearance K961036 for MBI FIBEROPTIC ENDO-ILLUMINATOR, Substantially Equivalent on 1996-07-15. Applicant: M.B. Industries, Inc.. Device class: 2.

Clearance details

Applicant: M.B. Industries, Inc.
Product code: Code MPA
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1996-03-14
Decision date: 1996-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Granite City, IL, US

Download summary PDF View on FDA.gov ↗

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