RIBOSOMAL P EIA TEST SYSTEM— 510(k) K950169

Substantially Equivalent

Hogan & Hartson

FDA 510(k) clearance K950169 for RIBOSOMAL P EIA TEST SYSTEM, Substantially Equivalent on 1996-05-23. Applicant: Hogan & Hartson.

Clearance details

Applicant: Hogan & Hartson
Product code: Code MQA
Advisory panel: Immunology
Date received: 1995-01-17
Decision date: 1996-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, D.C., DC, US

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