Instant-View LH Ovulation Predicting Test

FDA 510(k) K022829 · Alfa Scientific Designs, Inc.

Substantially Equivalent

510(k) numberK022829

Submission

Device name
Instant-View LH Ovulation Predicting Test
Applicant
Alfa Scientific Designs, Inc.
Poway, CA, US
Received
August 26, 2002
Decision date
November 5, 2002
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CEP – Radioimmunoassay, Luteinizing Hormone
Device class
Class I (low risk)
Regulation
21 CFR 862.1485
Specialty
Clinical Chemistry

Other 510(k)s with product code CEP

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K013582Maybe?Mom Mini Ovulation MicroscopeCEP · Traditional Maybe?Mom01/16/2003SE
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K013874Clearplane Easy Ovulation TestCEP · Traditional Unipath , Ltd.02/19/2002SE
K013323TCI-31 Lifelong Ovulation TesterCEP · Traditional Tci New York12/05/2001SE
K012252Quik-Check Ovulation PredictorCEP · Traditional ACON Laboratories, Inc.08/24/2001SE
K010244Sure Check Ovulation PredictorCEP · Traditional Chembio Diagnostic Systems, Inc.05/02/2001SE
K002867Inverness Medical Ovulation Predictor TestCEP · Special Selfcare, Inc.10/12/2000SE
K991466Early Ovulation Predictor (Cassette), One Step Ovulation Predictor (Cassette), Ovulation…CEP · Traditional Selfcare, Inc.05/25/1999SE
K991386Early Ovulation Predictor (Stick), One Step Ovulation Predictor (Stick), Ovulation…CEP · Traditional Selfcare, Inc.05/25/1999SE
K990249Ovustick LH Ovulation Predictor, Model 9030, Ovucard LH Ovulation Predictor, Model 9031CEP · Traditional Phamatech03/22/1999SE

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Questions and answers

When was Instant-View LH Ovulation Predicting Test cleared by the FDA?

Instant-View LH Ovulation Predicting Test (K022829) received a 510(k) decision of Substantially Equivalent on November 5, 2002, 71 days after the submission was received.

What is the product code of K022829?

The FDA product code is CEP – Radioimmunoassay, Luteinizing Hormone, a Class I (low risk) device regulated under 21 CFR 862.1485.