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

ULTRA LOW LEVEL IMMUNOGLOBULIN G

K Number: K761224 · Decision Apr 7, 1977
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
75
Applicant Total
29
Review Days
120

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Basic Information

Device Name
ULTRA LOW LEVEL IMMUNOGLOBULIN G
K Number
K761224
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5510
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Intl. Diagnostic Technology
Date Received
December 8, 1976
Decision Date
April 7, 1977
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

Similar 510(k) Clearances

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

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Other Clearances by Intl. Diagnostic Technology

K Number Device Name
K850591 FIAX TOXO-M ANTIBODIES TEST KIT
K843570 FIAX HAPTOGLOBIN TEST KIT
K843621 FIAX 420 DILUTOR
K843356 FIAX 100 FLUOROMETER
K842749 FIAX TOTAL IGE TEST KIT
K842071 FIAX TRANSFERRIN TEST KIT
K841174 RUBELLA ANTIBODY FLUOROIMMUNOASSAY
K840867 ALPHA-1-ANTITRYPSIN, FITC, ANTIGEN
K834140 ANTINUCLEAR ANTIBODY IMMUNOLOGICAL SYS
K833984 ANTINUCLEAR ANTIBODY IMMUNOLOGICAL
Search all 29 clearances from Intl. Diagnostic Technology →