CDT CYTOTOXI TEST— 510(k) K883560

Name: FDA 510(k) clearance K883560
Creator: U.S. Food and Drug Administration
Published: 1988-10-25

Substantially Equivalent

Advanced Clinical Diagnostics

FDA 510(k) clearance K883560 for CDT CYTOTOXI TEST, Substantially Equivalent on 1988-10-25. Applicant: Advanced Clinical Diagnostics. Device class: 1.

Clearance details

Applicant: Advanced Clinical Diagnostics
Product code: Code LLH
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1988-08-19
Decision date: 1988-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Toledo, OH, US

Download summary PDF View on FDA.gov ↗

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