FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ANTISERUM TO HUMAN APOLIPOPROTEIN A-I

K Number: K850691 · Decision Nov 1, 1985
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
49
Applicant Total
40
Review Days
253

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Basic Information

Device Name
ANTISERUM TO HUMAN APOLIPOPROTEIN A-I
K Number
K850691
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Kent Laboratories, Inc.
Date Received
February 21, 1985
Decision Date
November 1, 1985
Product Code
MSJ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
MSJ Apolipoproteins

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Other Clearances by Kent Laboratories, Inc.

K Number Device Name
K951966 HUMAN PREALBUMIN RADIAL IMMUNODIFFUSION KIT
K951967 HUMAN C1 INACTIVATOR OR C-1 ESTERASE INHIBITOR RADIAL IMMUNODIFFUSION KIT
K951968 HUMAN C1Q RADIAL IMMUNODIFFUSION KIT
K950102 HUMAN C-5 RADIAL IMMUNODIFFUSION KIT
K850683 72 DETERM. SIZE RADIAL IMMUNODIFFUSION TEST ALPHA2
K850682 72 DETERM. SIZE RADIAL IMMUNO. TEST HUMAN CERULOPL
K850690 ANTISERUM TO HUMAN APOLIPOPROTEIN B
K850686 ANTISERUM TO HUMAN PREALBUMIN
K831961 IMMUNODIFFUSION TEST HUMAN ANTITHROMBIN
K831958 RADIAL IMMUNO-TEST FOR HUMAN C-REACTI
Search all 40 clearances from Kent Laboratories, Inc. →