TINTELIZE PAI-1 KIT— 510(k) K960438

Substantially Equivalent

Medical Diagnostic Technologies, Inc.

FDA 510(k) clearance K960438 for TINTELIZE PAI-1 KIT, Substantially Equivalent on 1996-06-05. Applicant: Medical Diagnostic Technologies, Inc..

Clearance details

Applicant: Medical Diagnostic Technologies, Inc.
Product code: Code GGP
Advisory panel: Hematology
Date received: 1996-01-31
Decision date: 1996-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ventura, CA, US

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