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FDA 510(k)

PEAK OVULATION PREDICTOR

K-Number: K863121 · 1986-10-14

ApplicantMicron Technology, Inc.
Decision Date1986-10-14
Product CodeNGE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PEAK OVULATION PREDICTOR is the device name listed in this FDA 510(k) record. The listed applicant is Micron Technology, Inc.. It received FDA 510(k) clearance on 1986-10-14 under 510(k) number K863121. 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 PEAK OVULATION PREDICTOR?

PEAK OVULATION PREDICTOR is a medical device that received FDA 510(k) clearance on 1986-10-14. The listed applicant is Micron Technology, Inc.. The 510(k) number is K863121.

When did PEAK OVULATION PREDICTOR receive FDA 510(k) clearance?

PEAK OVULATION PREDICTOR received FDA 510(k) clearance on 1986-10-14, under 510(k) number K863121.

Who is the listed applicant for PEAK OVULATION PREDICTOR?

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

What is the FDA product code for PEAK OVULATION PREDICTOR?

The FDA product code for PEAK OVULATION PREDICTOR is NGE.

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Other records listing Micron Technology, Inc. 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.

K921167ULTRABLADE

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.K981207CLEARPLAN EASY FERTILITY MONITORUnipath , Ltd.K973860OVULON MONITORConception 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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