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

LDH S.C.E.

K Number: K863068 · Decision Dec 10, 1986
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
110
Applicant Total
34
Review Days
120

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Basic Information

Device Name
LDH S.C.E.
K Number
K863068
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1440
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
J. D. Assoc.
Date Received
August 12, 1986
Decision Date
December 10, 1986
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 J. D. Assoc.

K Number Device Name
K863103 PEG 6,000
K863054 AST S.C.E. (GOT)
K863069 MAGNESIOMETER
K863079 CREATINKINETIC
K863112 PROTEINMETER
K863053 ALT S.C.E. (GPT)
K863066 TRANSFERMETER
K863109 FERROFAST
K863102 GLUCOMETER-E
K863056 BILIRUBIN TOTAL
Search all 34 clearances from J. D. Assoc. →