510(k) K170222

Rapid Tox Cup II by American Bio Medica Corp. — Product Code LAF

K170222 is an FDA 510(k) premarket notification submitted by American Bio Medica Corp. for the device "Rapid Tox Cup II". The FDA issued a decision of Substantially Equivalent on August 15, 2017. The device falls under product code LAF (Gas Chromatography, Methamphetamine), a Class II device regulated under 21 CFR 862.3610. American Bio Medica Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 15, 2017
Date Received
January 25, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gas Chromatography, Methamphetamine
Device Class
Class II
Regulation Number
862.3610
Review Panel
TX
Submission Type