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

HICHEM LDH/L REAGENT KIT

K Number: K946022 · Decision Feb 23, 1995
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
110
Applicant Total
41
Review Days
73

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Basic Information

Device Name
HICHEM LDH/L REAGENT KIT
K Number
K946022
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1440
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hichem Diagnostics
Date Received
December 12, 1994
Decision Date
February 23, 1995
Product Code
CFJ
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
CFJ Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase

Similar 510(k) Clearances

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

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Other Clearances by Hichem Diagnostics

K Number Device Name
K981794 HICHEM CALCIUM REAGENT KIT
K963383 HICHEM ALP/AMP REAGENT KIT
K953862 HICHEM ISEKCI SOLUTION KIT 70010
K953860 HICHEM ISE DILUENT KIT 70008
K953861 HICHEM ISE INTDERNAL REFERENCE KIT 70009
K953863 HICHEM ISE STANDARDS KIT 70011
K951751 HICHEM AST REAGENT KIT
K946192 HICHEM Y-GT REAGENT KIT
K941433 HI CHEM AQUEOUS GLUCOSE CONTROL, LOW, MED, HIGH
K925612 HI CHEM ELECTROLYTE BUFFER
Search all 41 clearances from Hichem Diagnostics →