PREMIER C. DIFFICILE, MODIFICATION— 510(k) K926442

Name: FDA 510(k) clearance K926442
Creator: U.S. Food and Drug Administration
Published: 1993-01-27

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K926442 for PREMIER C. DIFFICILE, MODIFICATION, Substantially Equivalent on 1993-01-27. Applicant: Meridian Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code LLH
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1992-12-16
Decision date: 1993-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

Download summary PDF View on FDA.gov ↗

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