IMPROVED THAYER-MARTIN MEDIUM— 510(k) K770925

Name: FDA 510(k) clearance K770925
Creator: U.S. Food and Drug Administration
Published: 1977-06-08

Substantially Equivalent

Micro-Tech Diagnostic, Inc.

FDA 510(k) clearance K770925 for IMPROVED THAYER-MARTIN MEDIUM, Substantially Equivalent on 1977-06-08. Applicant: Micro-Tech Diagnostic, Inc.. Device class: 2.

Clearance details

Applicant: Micro-Tech Diagnostic, Inc.
Product code: Code JTY
Device class: Class 2
Regulation: 21 CFR 866.2410
Advisory panel: Microbiology
Date received: 1977-05-20
Decision date: 1977-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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