510(k) K063804

OLYMPUS TRIGLYCERIDE TEST SYSTEM by Olympus America, Inc. — Product Code CDT

K063804 is an FDA 510(k) premarket notification submitted by Olympus America, Inc. for the device "OLYMPUS TRIGLYCERIDE TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on March 23, 2007. The device falls under product code CDT (Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides), a Class I device regulated under 21 CFR 862.1705. Olympus America, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 23, 2007
Date Received
December 22, 2006
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