510(k) K033884

RANDOX AMIKACIN by Randox Laboratories, Ltd. — Product Code KLQ

K033884 is an FDA 510(k) premarket notification submitted by Randox Laboratories, Ltd. for the device "RANDOX AMIKACIN". The FDA issued a decision of Substantially Equivalent on June 9, 2004. The device falls under product code KLQ (Radioimmunoassay, Amikacin), a Class II device regulated under 21 CFR 862.3035. Randox Laboratories, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 9, 2004
Date Received
December 15, 2003
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Amikacin
Device Class
Class II
Regulation Number
862.3035
Review Panel
TX
Submission Type