LEUKO-TEST— 510(k) K951101

Substantially Equivalent

Techlab, Inc.

FDA 510(k) clearance K951101 for LEUKO-TEST, Substantially Equivalent on 1995-04-24. Applicant: Techlab, Inc..

Clearance details

Applicant: Techlab, Inc.
Product code: Code DEG
Advisory panel: Immunology
Date received: 1995-03-10
Decision date: 1995-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Blacksburg, VA, US

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