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

GILFORD IMMUNOGLOBULIN M REAGENT

K Number: K853469 · Decision Sep 16, 1985
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
32
Applicant Total
10
Review Days
28

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
GILFORD IMMUNOGLOBULIN M REAGENT
K Number
K853469
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5550
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Gilford
Date Received
August 19, 1985
Decision Date
September 16, 1985
Product Code
DFT
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
DFT Igm, Antigen, Antiserum, Control

Similar 510(k) Clearances

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

View all

Other Clearances by Gilford

K Number Device Name
K853465 GILFORD IMMUNOGLOBULIN G REAGENT
K853467 GILFORD IMMUNOGLOBULIN A REAGENT
K853468 GILFORD C4 COMPLEMENT REAGENT
K853466 GILFORD C3 COMPLEMENT REAGENT
K851202 GILFORD TRI-LEVEL ASSAYED IMMUNOLOGY CONTROL
K842500 DATA MGMT. SYSTEM
K840120 ADVANTAGE
K833067 IMPACT 400 #1447X2
K812787 EIA RUBELLA