FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

FIAGEN FERRITIN

K Number: K882822 · Decision Aug 4, 1988
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
2
Applicant Total
17
Review Days
27

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Basic Information

Device Name
FIAGEN FERRITIN
K Number
K882822
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5550
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Cyberfluor, Inc.
Date Received
July 8, 1988
Decision Date
August 4, 1988
Product Code
DFL
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
DFL Igm, Ferritin, Antigen, Antiserum, Control

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K895186 FIAGEN T3 UPTAKE CATALOGUE #101-402
K895396 CYBERFLUOR FIAGEN TSH
K884708 FIAGEN HFSH TIME-RESOLVED FLUOROIMMUNOASSAY KIT
K884707 FIAGEN DIGOXIN TIME-RESOLVED FLUOROIMMUNOASSAY KIT
K884201 FIAGEN TBG TIME-RESOLVED FLUOROIMMUNOASSAY KIT
K883182 FIAGEN RUBELLA IGG
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