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

LONDON DIAGNOSTICS LUMATAG (R) IGE CHEM. IMM ASSAY

K Number: K903195 · Decision Aug 2, 1990
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
113
Applicant Total
12
Review Days
14

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
LONDON DIAGNOSTICS LUMATAG (R) IGE CHEM. IMM ASSAY
K Number
K903195
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
London Diagnostics, Inc.
Date Received
July 19, 1990
Decision Date
August 2, 1990
Product Code
DGC
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
DGC Ige, Antigen, Antiserum, Control

Similar 510(k) Clearances

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

View all

Other Clearances by London Diagnostics, Inc.

K Number Device Name
K914835 LUMATAG FREE T4 CHEMILUMINESCENCE ASSAY
K911985 LUMATAG T4 CHEMILUMINESCENCE ASSAY
K912858 LONDON DIAGNOSTICS LUMATAG(R) HGH CHEM IMMUN ASSAY
K905814 LUMATAG(R) FSH CHEMILUMINESCENCE IMMUNOMETRI ASSAY
K904458 LUMATAG(TM) PROLACTIN DIAGNOSTIC KIT/MODIFICATION
K903130 LONDON DIAGNOSTICS LUMATAG(TM) INTACT PTH ASSAY
K902443 LUMATAG(TM) LH DIAGNOSTIC KIT
K901484 LUMATAG(TM) HCG CHEMILUMINESCENCE IMMUNOMETRIC
K901075 LUMATAG(TM) FERRITIN CHEMILUMINESCENCE IMMUNOMET.
K881443 LUMATAG(TM) TSH CHEMILUMINESCENCE IMMUNO. ASSAY
Search all 12 clearances from London Diagnostics, Inc. →