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FDA 510(k)

FETAL VITABILITY TM MODE

K-Number: K812743 · 1981-11-16

ApplicantTechnicare Corp.
Decision Date1981-11-16
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FETAL VITABILITY TM MODE is the device name listed in this FDA 510(k) record. The listed applicant is Technicare Corp.. It received FDA 510(k) clearance on 1981-11-16 under 510(k) number K812743. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FETAL VITABILITY TM MODE?

FETAL VITABILITY TM MODE is a medical device that received FDA 510(k) clearance on 1981-11-16. The listed applicant is Technicare Corp.. The 510(k) number is K812743.

When did FETAL VITABILITY TM MODE receive FDA 510(k) clearance?

FETAL VITABILITY TM MODE received FDA 510(k) clearance on 1981-11-16, under 510(k) number K812743.

Who is the listed applicant for FETAL VITABILITY TM MODE?

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

What is the FDA product code for FETAL VITABILITY TM MODE?

The FDA product code for FETAL VITABILITY TM MODE is IYO.

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Other records listing Technicare Corp. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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