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

RADIAL IMMUNO-DIFFUSION PLATES IGA, IGD, IGG & IGM

K Number: K851284 · Decision Jun 11, 1985
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
53
Applicant Total
19
Review Days
71

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
RADIAL IMMUNO-DIFFUSION PLATES IGA, IGD, IGG & IGM
K Number
K851284
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Cooper Biomedical, Inc.
Date Received
April 1, 1985
Decision Date
June 11, 1985
Product Code
CZP
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
CZP Iga, Antigen, Antiserum, Control

Similar 510(k) Clearances

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

View all

Other Clearances by Cooper Biomedical, Inc.

K Number Device Name
K863868 IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/ALPHA-1 ANT
K864512 IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/HUMAN HAPTO
K863301 DEMAND TOTAL PROTEIN
K861926 WORTHINGTON HDL PRECIPITATING REAGENT SET
K854130 DEMAND ETHYL ALCOHOL
K853949 DEMAND ACID PHOSPHATASE REAGENT
K852262 ASSIST CLINICAL CHEMISTRY ANALYZER
K851285 RADIAL IMMUNODIFFUSION PLATES CSF IGG & CSF ALBUMI
K851286 RADIAL IMMUNODIFFUSION PLATES C3 & C4
K851282 RADIAL IMMUNODIFFUSION PLATES ALPHA-2 MACROGLOBULI
Search all 19 clearances from Cooper Biomedical, Inc. →