FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

FIAGEN PROGESTERONE

K Number: K923410 · Decision Dec 3, 1992
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
56
Applicant Total
17
Review Days
146

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Basic Information

Device Name
FIAGEN PROGESTERONE
K Number
K923410
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1620
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cyberfluor, Inc.
Date Received
July 10, 1992
Decision Date
December 3, 1992
Product Code
JLS
Advisory Committee
Clinical Chemistry
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
JLS Radioimmunoassay, Progesterone

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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
K882823 FIAGEN HGH FLUOROIMMUNOASSAY KIT
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