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

GILFORD IMMUNOGLOBULIN G REAGENT

K Number: K853465 · Decision Sep 16, 1985
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
75
Applicant Total
10
Review Days
28

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Basic Information

Device Name
GILFORD IMMUNOGLOBULIN G REAGENT
K Number
K853465
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Gilford
Date Received
August 19, 1985
Decision Date
September 16, 1985
Product Code
DEW
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
DEW Igg, Antigen, Antiserum, Control

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Other Clearances by Gilford

K Number Device Name
K853467 GILFORD IMMUNOGLOBULIN A REAGENT
K853468 GILFORD C4 COMPLEMENT REAGENT
K853469 GILFORD IMMUNOGLOBULIN M 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