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.. Device class: 1.

Clearance details

Applicant: Techlab, Inc.
Product code: Code DEG
Device class: Class 1
Regulation: 21 CFR 866.5570
Advisory panel: Immunology
Date received: 1995-03-10
Decision date: 1995-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Blacksburg, VA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.