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FDA 510(k)

FETASONDE 5, #30, CENTRAL NURSING STAT

K-Number: K812863 · 1981-11-06

ApplicantKontron Instruments, Inc.
Decision Date1981-11-06
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FETASONDE 5, #30, CENTRAL NURSING STAT is the device name listed in this FDA 510(k) record. The listed applicant is Kontron Instruments, Inc.. It received FDA 510(k) clearance on 1981-11-06 under 510(k) number K812863. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FETASONDE 5, #30, CENTRAL NURSING STAT?

FETASONDE 5, #30, CENTRAL NURSING STAT is a medical device that received FDA 510(k) clearance on 1981-11-06. The listed applicant is Kontron Instruments, Inc.. The 510(k) number is K812863.

When did FETASONDE 5, #30, CENTRAL NURSING STAT receive FDA 510(k) clearance?

FETASONDE 5, #30, CENTRAL NURSING STAT received FDA 510(k) clearance on 1981-11-06, under 510(k) number K812863.

Who is the listed applicant for FETASONDE 5, #30, CENTRAL NURSING STAT?

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

What is the FDA product code for FETASONDE 5, #30, CENTRAL NURSING STAT?

The FDA product code for FETASONDE 5, #30, CENTRAL NURSING STAT is HGM.

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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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