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

SPQ TM TEST SYSTEM II FOR CRP

K Number: K892526 · Decision May 9, 1989
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
18
Review Days
28

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Basic Information

Device Name
SPQ TM TEST SYSTEM II FOR CRP
K Number
K892526
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Atlantic Antibodies
Date Received
April 11, 1989
Decision Date
May 9, 1989
Product Code
DCK
Advisory Committee
Immunology
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
DCK C-Reactive Protein, Antigen, Antiserum, And Control

Similar 510(k) Clearances

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Other Clearances by Atlantic Antibodies

K Number Device Name
K891154 SPQ(TM) ANTIBODY REAGENT SET II FOR APO A-I/APO B
K890563 SPQ(TM) ANTIBODY REAGENT SET II FOR TRF
K890561 SPQ(TM) ANTIBODY REAGENT SET II FOR IGM
K890562 SPQ(TM) ANTIBODY REAGENT SET II FOR HPT
K890416 SPQ(TM) ANTIBODY REAGENT SET II FOR IGG
K890564 SPQ(TM) ANTIBODY REAGENT SET II FOR C4
K890417 SPQ(TM) ANTIBODY REAGENT SET II FOR C3
K890415 SPQ(TM) ANTIBODY REAGENT SET II FOR AAT
K890560 SPQ(TM) ANTIBODY REAGENT SET II FOR IGA
K884297 SPQ(TM) TEST SYSTEM FOR PREALBUMIN
Search all 18 clearances from Atlantic Antibodies →