PATHODX CHLAMYDIA TRACHOMATIS DIRECT SPECIMEN TEST— 510(k) K900870

Substantially Equivalent

Diagnostic Products Corp.

FDA 510(k) clearance K900870 for PATHODX CHLAMYDIA TRACHOMATIS DIRECT SPECIMEN TEST, Substantially Equivalent on 1990-04-16. Applicant: Diagnostic Products Corp..

Clearance details

Applicant: Diagnostic Products Corp.
Product code: Code LJP
Advisory panel: Microbiology
Date received: 1990-02-24
Decision date: 1990-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

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