FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MODIFIED OVUGEN

K Number: K902208 · Decision Jul 17, 1990
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
142
Applicant Total
12
Review Days
62

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Basic Information

Device Name
MODIFIED OVUGEN
K Number
K902208
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1485
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Biogenex Laboratories
Date Received
May 16, 1990
Decision Date
July 17, 1990
Product Code
CEP
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CEP Radioimmunoassay, Luteinizing Hormone

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K925189 PREGNAGEN 1-STEP PREGNANCY TEST
K884880 PREGNAGEN(TM)
K882002 PREGNAGEN(TM)
K873534 OVUGEN SURETEST
K831221 RIAGEN B-HCG RIA KIT
K821657 RIAGEN B-HCG RIA
K821234 RIAGEN B-HCG RIA
K820724 FLUOROGEN PAP FIA
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