V.D.T.-GONORRHEA TEST KIT— 510(k) K840799

Substantially Equivalent

M.G. Laboratories, Inc.

FDA 510(k) clearance K840799 for V.D.T.-GONORRHEA TEST KIT, Substantially Equivalent on 1984-06-07. Applicant: M.G. Laboratories, Inc.. Device class: 1.

Clearance details

Applicant
M.G. Laboratories, Inc.
Product code
Code LIO
Device class
Class 1
Regulation
21 CFR 866.2900
Advisory panel
Microbiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Walker, MI, US
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