MARTIN LEWIS TRANSGROW— 510(k) K771872

Name: FDA 510(k) clearance K771872
Creator: U.S. Food and Drug Administration
Published: 1977-10-25

Substantially Equivalent

Granite Diagnostics, Inc.

FDA 510(k) clearance K771872 for MARTIN LEWIS TRANSGROW, Substantially Equivalent on 1977-10-25. Applicant: Granite Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Granite Diagnostics, Inc.
Product code: Code JTY
Device class: Class 2
Regulation: 21 CFR 866.2410
Advisory panel: Microbiology
Date received: 1977-10-04
Decision date: 1977-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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