RAPIDONE - MARIJUANA TEST— 510(k) K990818

Substantially Equivalent

American Bio Medica Corp.

FDA 510(k) clearance K990818 for RAPIDONE - MARIJUANA TEST, Substantially Equivalent on 1999-07-07. Applicant: American Bio Medica Corp.. Device class: 2.

Clearance details

Applicant
American Bio Medica Corp.
Product code
Code LDJ
Device class
Class 2
Regulation
21 CFR 862.3870
Advisory panel
Clinical Toxicology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Washington, DC, US
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