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

LUMATAG(TM) FERRITIN CHEMILUMINESCENCE IMMUNOMET.

K Number: K901075 · Decision Apr 2, 1990
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
86
Applicant Total
12
Review Days
25

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Basic Information

Device Name
LUMATAG(TM) FERRITIN CHEMILUMINESCENCE IMMUNOMET.
K Number
K901075
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5340
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
London Diagnostics, Inc.
Date Received
March 8, 1990
Decision Date
April 2, 1990
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

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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
K903195 LONDON DIAGNOSTICS LUMATAG (R) IGE CHEM. IMM ASSAY
K901484 LUMATAG(TM) HCG CHEMILUMINESCENCE IMMUNOMETRIC
K881443 LUMATAG(TM) TSH CHEMILUMINESCENCE IMMUNO. ASSAY
Search all 12 clearances from London Diagnostics, Inc. →