OPUS RUBELLA TEST SYSTEM— 510(k) K915870

Substantially Equivalent

Pb Diagnostics, Inc.

FDA 510(k) clearance K915870 for OPUS RUBELLA TEST SYSTEM, Substantially Equivalent on 1992-03-23. Applicant: Pb Diagnostics, Inc..

Clearance details

Applicant: Pb Diagnostics, Inc.
Product code: Code LFX
Advisory panel: Microbiology
Date received: 1991-12-31
Decision date: 1992-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westwood, MA, US

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