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FDA 510(k)

FERTILITE OV

K-Number: K020808 · 2002-09-23

ApplicantPheromone Sciences Corp.
Decision Date2002-09-23
Product CodeNGE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FERTILITE OV is the device name listed in this FDA 510(k) record. The listed applicant is Pheromone Sciences Corp.. It received FDA 510(k) clearance on 2002-09-23 under 510(k) number K020808. The device is classified under product code NGE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FERTILITE OV?

FERTILITE OV is a medical device that received FDA 510(k) clearance on 2002-09-23. The listed applicant is Pheromone Sciences Corp.. The 510(k) number is K020808.

When did FERTILITE OV receive FDA 510(k) clearance?

FERTILITE OV received FDA 510(k) clearance on 2002-09-23, under 510(k) number K020808.

Who is the listed applicant for FERTILITE OV?

The FDA 510(k) record lists Pheromone Sciences Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FERTILITE OV?

The FDA product code for FERTILITE OV is NGE.

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Related Devices (Code: NGE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K990223MODIFICATION OF CLEARPLAN EASY FERTILITY MONITORUnipath , Ltd.K981207CLEARPLAN EASY FERTILITY MONITORUnipath , Ltd.K973860OVULON MONITORConception Technology, Inc.K863121PEAK OVULATION PREDICTORMicron Technology, Inc.K850579CUE FERTILITY MONITORZetek, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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