MICROCON 800MUV, MICROCON 400MUV, MICROCON EXC-BUV— 510(k) K972064

Name: FDA 510(k) clearance K972064
Creator: U.S. Food and Drug Administration
Published: 1997-12-01

Substantially Equivalent

Biological Controls, Inc.

FDA 510(k) clearance K972064 for MICROCON 800MUV, MICROCON 400MUV, MICROCON EXC-BUV, Substantially Equivalent on 1997-12-01. Applicant: Biological Controls, Inc.. Device class: 2.

Clearance details

Applicant: Biological Controls, Inc.
Product code: Code FRA
Device class: Class 2
Regulation: 21 CFR 880.6500
Advisory panel: General Hospital
Date received: 1997-06-03
Decision date: 1997-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eatontown, NJ, US

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