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

OVUSTICK LH OVULATION PREDICTOR, MODEL 9030, OVUCARD LH OVULATION PREDICTOR, MODEL 9031

K Number: K990249 · Decision Mar 22, 1999
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
142
Applicant Total
47
Review Days
55

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Basic Information

Device Name
OVUSTICK LH OVULATION PREDICTOR, MODEL 9030, OVUCARD LH OVULATION PREDICTOR, MODEL 9031
K Number
K990249
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1485
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Phamatech
Date Received
January 26, 1999
Decision Date
March 22, 1999
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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