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

SPQ(TM) ANTIBODY REAGENT SET II FOR TRF

K Number: K890563 · Decision Mar 3, 1989
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
47
Applicant Total
18
Review Days
38

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Basic Information

Device Name
SPQ(TM) ANTIBODY REAGENT SET II FOR TRF
K Number
K890563
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5880
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Atlantic Antibodies
Date Received
January 24, 1989
Decision Date
March 3, 1989
Product Code
DDG
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
DDG Transferrin, Antigen, Antiserum, Control

Similar 510(k) Clearances

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Other Clearances by Atlantic Antibodies

K Number Device Name
K892526 SPQ TM TEST SYSTEM II FOR CRP
K891154 SPQ(TM) ANTIBODY REAGENT SET II FOR APO A-I/APO B
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 →