'RAPIDONE'-METHADONE TEST— 510(k) K012164

Substantially Equivalent

American Bio Medica Corp.

FDA 510(k) clearance K012164 for 'RAPIDONE'-METHADONE TEST, Substantially Equivalent on 2001-11-20. Applicant: American Bio Medica Corp..

Clearance details

Applicant: American Bio Medica Corp.
Product code: Code DJR
Advisory panel: Clinical Toxicology
Date received: 2001-07-11
Decision date: 2001-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia, MD, US

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