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

LACTATE DEHYDROGENASE CAT. # 320-68, 320-69

K Number: K875206 · Decision Feb 2, 1988
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
110
Applicant Total
77
Review Days
46

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Basic Information

Device Name
LACTATE DEHYDROGENASE CAT. # 320-68, 320-69
K Number
K875206
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1440
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Diagnostic Chemicals, Ltd. (Usa)
Date Received
December 18, 1987
Decision Date
February 2, 1988
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

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Other Clearances by Diagnostic Chemicals, Ltd. (Usa)

K Number Device Name
K022538 IMMUNODIP URINARY ALBUMIN SCREEN ASSAY, CATALOGUE NUMBER 790-25
K974874 BILIRUBIN-SL (TOTAL) ASSAY
K932556 AMMONIA ASSAY CAT. NO. 200-02
K932766 HDL-CHOLESTRAL(DEXTRAN SULFATE/MAGNESIUM)
K932555 DC-LINEATE CAT. NO. SE-091
K925877 DC-UIBC-CAL
K912825 MAGNESIUM ASSAY KIT, CAT.# 100-12
K895964 DCL SYPHILIS-M CATALOG NO. 600-80
K895965 DCL - SYPHILIS-G ASSAY CATALOG NO. 600-70
K904660 ENZYMATIC BILIRUBIN (TOTAL), CATALOGUE NO. 202-14
Search all 77 clearances from Diagnostic Chemicals, Ltd. (Usa) →