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

ANSWER OVULATION TEST KIT

K Number: K871241 · Decision Oct 2, 1987
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
142
Applicant Total
68
Review Days
189

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Basic Information

Device Name
ANSWER OVULATION TEST KIT
K Number
K871241
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1485
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Armkel, LLC
Date Received
March 27, 1987
Decision Date
October 2, 1987
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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K001212 TROJAN EXTRA LARGE LATEX CONDOM
K000748 TROJAN LATEX CONDOM WITH MALE GENITAL DESENSITIZER LUBRICANT
K992232 FIRST RESPONSE 1-STEP PREGNANCY
K973352 BRAND NAME *1-STEP PREGNANCY
K973310 TBD* ONE-STEP OVULATION PREDICTOR TEST
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