FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CREATINE KINASE REAGENT CK LTS

K Number: K831965 · Decision Sep 12, 1983
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
122
Applicant Total
41
Review Days
84

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Basic Information

Device Name
CREATINE KINASE REAGENT CK LTS
K Number
K831965
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Electro-Nucleonics Laboratories, Inc.
Date Received
June 20, 1983
Decision Date
September 12, 1983
Product Code
CGS
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
CGS Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes

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Other Clearances by Electro-Nucleonics Laboratories, Inc.

K Number Device Name
K873925 VIRGO(TM) MEASLES IGG ELISA
K873617 GEMSTAR II SYSTEM
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
K863874 LIPASE HYDROLYSIS/GLYCEROL KINASE, TRIGLYCERIDES
K862640 AMYLASE LTS
K853372 GEMSTAR IPA THEOPHYLLINE TEST KIT
Search all 41 clearances from Electro-Nucleonics Laboratories, Inc. →