BIOTRACK PHENYTOIN TEST CARTRIDGE— 510(k) K915755

Substantially Equivalent

Biotrack, Inc.

FDA 510(k) clearance K915755 for BIOTRACK PHENYTOIN TEST CARTRIDGE, Substantially Equivalent on 1992-07-23. Applicant: Biotrack, Inc..

Clearance details

Applicant: Biotrack, Inc.
Product code: Code DIP
Advisory panel: Clinical Toxicology
Date received: 1991-12-23
Decision date: 1992-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountain View, CA, US

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