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FDA 510(k)

TCOYF FERTILITY SOFTWARE VERSION 1.0

K-Number: K002726 · 2001-04-06

ApplicantOvusoft, LLC
Decision Date2001-04-06
Product CodeLHD
DecisionSubstantially Equivalent

Device Summary

TCOYF FERTILITY SOFTWARE VERSION 1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Ovusoft, LLC. It received FDA 510(k) clearance on 2001-04-06 under 510(k) number K002726. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TCOYF FERTILITY SOFTWARE VERSION 1.0?

TCOYF FERTILITY SOFTWARE VERSION 1.0 is a medical device that received FDA 510(k) clearance on 2001-04-06. The listed applicant is Ovusoft, LLC. The 510(k) number is K002726.

When did TCOYF FERTILITY SOFTWARE VERSION 1.0 receive FDA 510(k) clearance?

TCOYF FERTILITY SOFTWARE VERSION 1.0 received FDA 510(k) clearance on 2001-04-06, under 510(k) number K002726.

Who is the listed applicant for TCOYF FERTILITY SOFTWARE VERSION 1.0?

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

What is the FDA product code for TCOYF FERTILITY SOFTWARE VERSION 1.0?

The FDA product code for TCOYF FERTILITY SOFTWARE VERSION 1.0 is LHD.

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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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