510(k) K092266

RANDOX METHAMPHETAMINE ASSAY by Randox Laboratories, Ltd. — Product Code DKB

K092266 is an FDA 510(k) premarket notification submitted by Randox Laboratories, Ltd. for the device "RANDOX METHAMPHETAMINE ASSAY". The FDA issued a decision of Substantially Equivalent on May 9, 2011. The device falls under product code DKB (Calibrators, Drug Mixture), a Class II device regulated under 21 CFR 862.3200. Randox Laboratories, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 9, 2011
Date Received
July 28, 2009
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Calibrators, Drug Mixture
Device Class
Class II
Regulation Number
862.3200
Review Panel
TX
Submission Type