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

TRIGLYCERIDES - GPO REAGENT

K Number: K890337 · Decision Mar 9, 1989
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
33
Review Days
45

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
TRIGLYCERIDES - GPO REAGENT
K Number
K890337
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Alpkem Corp.
Date Received
January 23, 1989
Decision Date
March 9, 1989
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CDT), ordered by most recent decision date.

View all

Other Clearances by Alpkem Corp.

K Number Device Name
K894011 TOTAL GALACTOSE
K891070 PHENYLALANINE (NINHYDRIN REACTION)
K890334 TOTAL CHOLESTEROL REAGENT
K890336 GLUCOSE (GOD) REAGENT
K890332 RFA/2 RAPID FLOW ANALYZER W/COMPUTER
K890335 SODIUM HYDROXIDE SOLUTION, CREATININE REAG./DILU.
K890333 ALBUMIN REAGENT
K883020 RFA-300 RAPID FLOW ANALYZER W/COMPUTER
K860367 MAGNESIUM (SUBSTRATE, ENZYME, REAGENT)
K851990 INTERNAL STANDARD SOLUTION, EXTERNAL STANDARD SOLU
Search all 33 clearances from Alpkem Corp. →