510(k) K060355

ACRO BIOTECH LLC RAPID MDMA URINE TEST, CATALOG MDMA0010000 by Acro Biotech, LLC — Product Code DJC

K060355 is an FDA 510(k) premarket notification submitted by Acro Biotech, LLC for the device "ACRO BIOTECH LLC RAPID MDMA URINE TEST, CATALOG MDMA0010000". The FDA issued a decision of Substantially Equivalent on August 7, 2006. The device falls under product code DJC (Thin Layer Chromatography, Methamphetamine), a Class II device regulated under 21 CFR 862.3610. Acro Biotech, LLC has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 7, 2006
Date Received
February 13, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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