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

KINASE ISOENZYME

K Number: K943024 · Decision Aug 2, 1994
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
37
Applicant Total
28
Review Days
68

Basic Information

Device Name
KINASE ISOENZYME
K Number
K943024
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
DUPONT MEDICAL PRODUCTS
Date Received
May 26, 1994
Decision Date
August 2, 1994
Product Code
JHS
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
JHS Differential Rate Kinetic Method, Cpk Or Isoenzymes

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Other Clearances by DUPONT MEDICAL PRODUCTS

K Number Device Name
K952815 DUPONT LIPASE CALIBRATOR
K950920 DUPONT DIMENSION TOTAL PROTEIN METHOD
K952816 LIPASE FLEX REAGENT CARTRIDGE
K952412 DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL
K945280 DUPONT DIMENSION C-REACTIVE PROTEIN METHOD
K944932 PHENOBARBITAL FLEX REAGENT CARTRIDGE
K941050 DUPONT ACA STAR
K943996 DUPONT ACA PLUS LUTEINIZING HORMONE (LH) METHOD
K941146 DUPONT ACA PLUS THYROID STIMULATING HORMONE SYSTEM
K942640 DUPONT DIMENSION AMYLASE METHOD
Search all 28 clearances from DUPONT MEDICAL PRODUCTS →