510(k) K863874

LIPASE HYDROLYSIS/GLYCEROL KINASE, TRIGLYCERIDES by Electro-Nucleonics Laboratories, Inc. — Product Code CDT

K863874 is an FDA 510(k) premarket notification submitted by Electro-Nucleonics Laboratories, Inc. for the device "LIPASE HYDROLYSIS/GLYCEROL KINASE, TRIGLYCERIDES". The FDA issued a decision of Substantially Equivalent on November 13, 1986. The device falls under product code CDT (Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides), a Class I device regulated under 21 CFR 862.1705. Electro-Nucleonics Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 13, 1986
Date Received
October 3, 1986
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