IS-RUBELLA IGG TEST SYSTEM— 510(k) K981729

Substantially Equivalent

Diamedix Corp.

FDA 510(k) clearance K981729 for IS-RUBELLA IGG TEST SYSTEM, Substantially Equivalent on 1999-01-28. Applicant: Diamedix Corp..

Clearance details

Applicant: Diamedix Corp.
Product code: Code LFX
Advisory panel: Microbiology
Date received: 1998-05-15
Decision date: 1999-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

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