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FDA 510(k)

FERTILITY FORECASTER COMPUTER PROGRAM

K-Number: K880618 · 1988-06-24

Decision Date1988-06-24
Product CodeLHD
DecisionSubstantially Equivalent

Device Summary

FERTILITY FORECASTER COMPUTER PROGRAM is the device name listed in this FDA 510(k) record. The listed applicant is Fertile Time, Ltd.. It received FDA 510(k) clearance on 1988-06-24 under 510(k) number K880618. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FERTILITY FORECASTER COMPUTER PROGRAM?

FERTILITY FORECASTER COMPUTER PROGRAM is a medical device that received FDA 510(k) clearance on 1988-06-24. The listed applicant is Fertile Time, Ltd.. The 510(k) number is K880618.

When did FERTILITY FORECASTER COMPUTER PROGRAM receive FDA 510(k) clearance?

FERTILITY FORECASTER COMPUTER PROGRAM received FDA 510(k) clearance on 1988-06-24, under 510(k) number K880618.

Who is the listed applicant for FERTILITY FORECASTER COMPUTER PROGRAM?

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

What is the FDA product code for FERTILITY FORECASTER COMPUTER PROGRAM?

The FDA product code for FERTILITY FORECASTER COMPUTER PROGRAM is LHD.

Related Clinical Trials

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.

Related Devices (Code: LHD)

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.

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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