DTM (DERMATOPHYTE TEST MEDIUM) AGAR— 510(k) K791414

Name: FDA 510(k) clearance K791414
Creator: U.S. Food and Drug Administration
Published: 1979-10-17

Substantially Equivalent

Biomedia, Inc.

FDA 510(k) clearance K791414 for DTM (DERMATOPHYTE TEST MEDIUM) AGAR, Substantially Equivalent on 1979-10-17. Applicant: Biomedia, Inc.. Device class: 1.

Clearance details

Applicant: Biomedia, Inc.
Product code: Code JSI
Device class: Class 1
Regulation: 21 CFR 866.2360
Advisory panel: Microbiology
Date received: 1979-07-30
Decision date: 1979-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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