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

CYBERFLUOR FIAGEN TSH

K Number: K895396 · Decision Oct 31, 1989
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
17
Review Days
60

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Basic Information

Device Name
CYBERFLUOR FIAGEN TSH
K Number
K895396
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Cyberfluor, Inc.
Date Received
September 1, 1989
Decision Date
October 31, 1989
Product Code
JLW
Advisory Committee
Clinical Chemistry
Review Advisory Committee
TX
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JLW Radioimmunoassay, Thyroid-Stimulating Hormone

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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
K882823 FIAGEN HGH FLUOROIMMUNOASSAY KIT
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