FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LIPASE HYDROLYSIS/GLYCEROL KINASE, TRIGLYCERIDES

K Number: K863874 · Decision Nov 13, 1986
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
41
Review Days
41

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Basic Information

Device Name
LIPASE HYDROLYSIS/GLYCEROL KINASE, TRIGLYCERIDES
K Number
K863874
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Electro-Nucleonics Laboratories, Inc.
Date Received
October 3, 1986
Decision Date
November 13, 1986
Product Code
CDT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CDT Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides

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Other Clearances by Electro-Nucleonics Laboratories, Inc.

K Number Device Name
K873925 VIRGO(TM) MEASLES IGG ELISA
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K873416 MULTI-ACCESS REAGENT DISPENSER
K873358 GEMENI URIC ACID U.V.
K873088 VIRGO(TM) RUBELLA IGG ELISA
K871905 TOXOPLASMA GONDII IGG ELISA
K870928 CHOLESTEROL (TOTAL) ANALYSIS PRODUCTS
K862640 AMYLASE LTS
K853372 GEMSTAR IPA THEOPHYLLINE TEST KIT
K853373 DELTA TROL I & II
Search all 41 clearances from Electro-Nucleonics Laboratories, Inc. →