MERITEC(TM)-CAMPY (JCL)— 510(k) K880389

Name: FDA 510(k) clearance K880389
Creator: U.S. Food and Drug Administration
Published: 1988-04-12

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K880389 for MERITEC(TM)-CAMPY (JCL), Substantially Equivalent on 1988-04-12. Applicant: Meridian Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code LQP
Device class: Class 1
Regulation: 21 CFR 866.3110
Advisory panel: Microbiology
Date received: 1988-01-28
Decision date: 1988-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

Download summary PDF View on FDA.gov ↗

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