FINGERPRINT-DOA— 510(k) K942836

Substantially Equivalent

Fingerprint Bioteck, Inc.

FDA 510(k) clearance K942836 for FINGERPRINT-DOA, Substantially Equivalent on 1995-05-01. Applicant: Fingerprint Bioteck, Inc.. Device class: 2.

Clearance details

Applicant: Fingerprint Bioteck, Inc.
Product code: Code DKZ
Device class: Class 2
Regulation: 21 CFR 862.3100
Advisory panel: Clinical Toxicology
Date received: 1994-06-15
Decision date: 1995-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairfax, VA, US

Download summary PDF View on FDA.gov ↗

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