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FDA 510(k)

COROMETRICS FETAL MONITOR 142

K-Number: K843918 · 1984-12-17

ApplicantGe Medical Systems Information Technologies
Decision Date1984-12-17
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

COROMETRICS FETAL MONITOR 142 is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Information Technologies. It received FDA 510(k) clearance on 1984-12-17 under 510(k) number K843918. 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 COROMETRICS FETAL MONITOR 142?

COROMETRICS FETAL MONITOR 142 is a medical device that received FDA 510(k) clearance on 1984-12-17. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K843918.

When did COROMETRICS FETAL MONITOR 142 receive FDA 510(k) clearance?

COROMETRICS FETAL MONITOR 142 received FDA 510(k) clearance on 1984-12-17, under 510(k) number K843918.

Who is the listed applicant for COROMETRICS FETAL MONITOR 142?

The FDA 510(k) record lists Ge Medical Systems Information Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COROMETRICS FETAL MONITOR 142?

The FDA product code for COROMETRICS FETAL MONITOR 142 is HGM.

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Other records listing Ge Medical Systems Information Technologies as applicant

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Related Devices (Code: 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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