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

COULTER CLONE GAM-FITC POLY ANTI (IGG & IGM)

K Number: K893419 · Decision Aug 3, 1989
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
75
Applicant Total
16
Review Days
93

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
COULTER CLONE GAM-FITC POLY ANTI (IGG & IGM)
K Number
K893419
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Coulter Immunology
Date Received
May 2, 1989
Decision Date
August 3, 1989
Product Code
DEW
Advisory Committee
Immunology
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
DEW Igg, Antigen, Antiserum, Control

Similar 510(k) Clearances

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

View all

Other Clearances by Coulter Immunology

K Number Device Name
K922744 CYTO-STAT/COULTER CLONE CD 3(IGG1)-FITC/T8-RD1
K922745 CYTO-STAT/COULTER CLONE CD3(IGG1)-FITC/T4-RD1
K910473 CYTO-STAT(R)/COULTER CLONE(R) T11-RD1/B4-FITC
K911793 COULTERCLONE
K893853 COULTER CLONE T8 MONOCLONAL ANTIBODY
K893852 COULTER CLONE T4 MONOCLONAL ANTIBODY
K894179 COULTER CLONE(R) MY4 MONOCLONAL ANTIBODY
K895917 CYTO-STAT/COULTER CLONE T4-RD1/T8-FITC MONO ANTI
K884605 COULTER CLONE MO2
K884020 COULTER CLONE B4 MONOCLONAL ANTIBODY
Search all 16 clearances from Coulter Immunology →