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FDA 510(k)

SYMPTOTHERM 8 FERTILITY INDICATOR

K-Number: K821507 · 1982-10-14

ApplicantOvix Corp., Inc.
Decision Date1982-10-14
Product CodeLHD
DecisionSubstantially Equivalent

Device Summary

SYMPTOTHERM 8 FERTILITY INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ovix Corp., Inc.. It received FDA 510(k) clearance on 1982-10-14 under 510(k) number K821507. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYMPTOTHERM 8 FERTILITY INDICATOR?

SYMPTOTHERM 8 FERTILITY INDICATOR is a medical device that received FDA 510(k) clearance on 1982-10-14. The listed applicant is Ovix Corp., Inc.. The 510(k) number is K821507.

When did SYMPTOTHERM 8 FERTILITY INDICATOR receive FDA 510(k) clearance?

SYMPTOTHERM 8 FERTILITY INDICATOR received FDA 510(k) clearance on 1982-10-14, under 510(k) number K821507.

Who is the listed applicant for SYMPTOTHERM 8 FERTILITY INDICATOR?

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

What is the FDA product code for SYMPTOTHERM 8 FERTILITY INDICATOR?

The FDA product code for SYMPTOTHERM 8 FERTILITY INDICATOR 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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