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FDA 510(k)

FERTILITY AWARENESS METHOD KIT

K-Number: K801791 · 1980-10-31

ApplicantTelesis Corp.
Decision Date1980-10-31
Product CodeFLK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FERTILITY AWARENESS METHOD KIT is the device name listed in this FDA 510(k) record. The listed applicant is Telesis Corp.. It received FDA 510(k) clearance on 1980-10-31 under 510(k) number K801791. The device is classified under product code FLK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FERTILITY AWARENESS METHOD KIT?

FERTILITY AWARENESS METHOD KIT is a medical device that received FDA 510(k) clearance on 1980-10-31. The listed applicant is Telesis Corp.. The 510(k) number is K801791.

When did FERTILITY AWARENESS METHOD KIT receive FDA 510(k) clearance?

FERTILITY AWARENESS METHOD KIT received FDA 510(k) clearance on 1980-10-31, under 510(k) number K801791.

Who is the listed applicant for FERTILITY AWARENESS METHOD KIT?

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

What is the FDA product code for FERTILITY AWARENESS METHOD KIT?

The FDA product code for FERTILITY AWARENESS METHOD KIT is FLK.

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Related Devices (Code: FLK)

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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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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