N-ASSAY TIA APO A1 TEST KIT— 510(k) K964292

Substantially Equivalent

Crestat Diagnostics, Inc.

FDA 510(k) clearance K964292 for N-ASSAY TIA APO A1 TEST KIT, Substantially Equivalent on 1997-08-01. Applicant: Crestat Diagnostics, Inc..

Clearance details

Applicant: Crestat Diagnostics, Inc.
Product code: Code DER
Advisory panel: Immunology
Date received: 1996-10-29
Decision date: 1997-08-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Murrieta, CA, US

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