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

DUPONT ACA(R) PLUS IMMUNOASSAY SYS FERRITIN(FERR) METH

K Number: K935528 · Decision Jan 28, 1994
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
86
Applicant Total
253
Review Days
73

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
DUPONT ACA(R) PLUS IMMUNOASSAY SYS FERRITIN(FERR) METH
K Number
K935528
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5340
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
E.I. Dupont DE Nemours & Co., Inc.
Date Received
November 16, 1993
Decision Date
January 28, 1994
Product Code
DBF
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
DBF Ferritin, Antigen, Antiserum, Control

Similar 510(k) Clearances

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

View all

Other Clearances by E.I. Dupont DE Nemours & Co., Inc.

K Number Device Name
K951851 ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAY
K953725 CRONEX RADIATION THERAPY VERIFICATION CASSETTE
K953724 CRONEX RADIATION THERAPY CASSETTE
K951441 DUPONT ACA DIGOXIN (DGN A) METHOD
K950137 URINE BARBITURATES SCREEN FLEX(TM) REAGENT CARTRIDGE
K950136 URINE OPIATES SCREEN FLEX(TM) REAGENT CARTRIDGE
K950181 URINE CANNABINOIDS SCREEN FLEX(TM) REAGENT CARTRIDGE
K950135 URINE AMPHETAMINES SCREEN FLEX(TM) REAGENT CARTRIDGE
K950182 URINE METHADONE SCREEN FLEX(TM) REAGENT CARTRIDGE
K950134 URINE COCAINE METABOLITE SCREEN FLEX(TM) REAGENT CATRIDGE
Search all 253 clearances from E.I. Dupont DE Nemours & Co., Inc. →