OVUSTICK LH OVULATION PREDICTOR, MODEL 9030, OVUCARD LH OVULATION PREDICTOR, MODEL 9031— 510(k) K990249

Name: FDA 510(k) clearance K990249
Creator: U.S. Food and Drug Administration
Published: 1999-03-22

Substantially Equivalent

Phamatech

FDA 510(k) clearance K990249 for OVUSTICK LH OVULATION PREDICTOR, MODEL 9030, OVUCARD LH OVULATION PREDICTOR, MODEL 9031, Substantially Equivalent on 1999-03-22. Applicant: Phamatech. Device class: 1.

Clearance details

Applicant: Phamatech
Product code: Code CEP
Device class: Class 1
Regulation: 21 CFR 862.1485
Advisory panel: Clinical Chemistry
Date received: 1999-01-26
Decision date: 1999-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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