DERMATOPHYTE TEST MEDIUM— 510(k) K822131

Name: FDA 510(k) clearance K822131
Creator: U.S. Food and Drug Administration
Published: 1982-08-03

Substantially Equivalent

Granite Diagnostics, Inc.

FDA 510(k) clearance K822131 for DERMATOPHYTE TEST MEDIUM, Substantially Equivalent on 1982-08-03. Applicant: Granite Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Granite Diagnostics, Inc.
Product code: Code JSD
Device class: Class 1
Regulation: 21 CFR 866.2360
Advisory panel: Microbiology
Date received: 1982-07-19
Decision date: 1982-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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