510(k) K993466

WAKO L-TYPE TRIGLYCERIDE TEST by Wako Chemicals USA, Inc. — Product Code CDT

K993466 is an FDA 510(k) premarket notification submitted by Wako Chemicals USA, Inc. for the device "WAKO L-TYPE TRIGLYCERIDE TEST". The FDA issued a decision of Substantially Equivalent on November 9, 1999. The device falls under product code CDT (Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides), a Class I device regulated under 21 CFR 862.1705. Wako Chemicals USA, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 9, 1999
Date Received
October 13, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides
Device Class
Class I
Regulation Number
862.1705
Review Panel
CH
Submission Type