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

DCL - SYPHILIS-G ASSAY CATALOG NO. 600-70

K Number: K895965 · Decision Dec 26, 1990
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
34
Applicant Total
77
Review Days
441

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Basic Information

Device Name
DCL - SYPHILIS-G ASSAY CATALOG NO. 600-70
K Number
K895965
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3830
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Diagnostic Chemicals, Ltd. (Usa)
Date Received
October 11, 1989
Decision Date
December 26, 1990
Product Code
LIP
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LIP Enzyme Linked Immunoabsorption Assay, Treponema Pallidum

Similar 510(k) Clearances

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

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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
K904660 ENZYMATIC BILIRUBIN (TOTAL), CATALOGUE NO. 202-14
K901510 ENZYMATIC THEOPHYLLINE REAGENT, #500-82
Search all 77 clearances from Diagnostic Chemicals, Ltd. (Usa) →