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FDA 510(k)

CLEARPLAN EASY FERTILITY MONITOR

K-Number: K981207 · 1998-10-28

ApplicantUnipath , Ltd.
Decision Date1998-10-28
Product CodeNGE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CLEARPLAN EASY FERTILITY MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Unipath , Ltd.. It received FDA 510(k) clearance on 1998-10-28 under 510(k) number K981207. 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 CLEARPLAN EASY FERTILITY MONITOR?

CLEARPLAN EASY FERTILITY MONITOR is a medical device that received FDA 510(k) clearance on 1998-10-28. The listed applicant is Unipath , Ltd.. The 510(k) number is K981207.

When did CLEARPLAN EASY FERTILITY MONITOR receive FDA 510(k) clearance?

CLEARPLAN EASY FERTILITY MONITOR received FDA 510(k) clearance on 1998-10-28, under 510(k) number K981207.

Who is the listed applicant for CLEARPLAN EASY FERTILITY MONITOR?

The FDA 510(k) record lists Unipath , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEARPLAN EASY FERTILITY MONITOR?

The FDA product code for CLEARPLAN EASY FERTILITY MONITOR is NGE.

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Other records listing Unipath , Ltd. as applicant

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.

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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.

K020808FERTILITE OVPheromone Sciences Corp.K990223MODIFICATION OF CLEARPLAN EASY FERTILITY MONITORUnipath , Ltd.K973860OVULON MONITORConception Technology, Inc.K863121PEAK OVULATION PREDICTORMicron Technology, Inc.K850579CUE FERTILITY MONITORZetek, Inc.

Official Source

View on FDA Database →

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

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