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FDA 510(k)

MONITOR, OFFICE MODEL 140

K-Number: K790139 · 1979-02-16

ApplicantGe Medical Systems Information Technologies
Decision Date1979-02-16
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MONITOR, OFFICE MODEL 140 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 1979-02-16 under 510(k) number K790139. 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 MONITOR, OFFICE MODEL 140?

MONITOR, OFFICE MODEL 140 is a medical device that received FDA 510(k) clearance on 1979-02-16. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K790139.

When did MONITOR, OFFICE MODEL 140 receive FDA 510(k) clearance?

MONITOR, OFFICE MODEL 140 received FDA 510(k) clearance on 1979-02-16, under 510(k) number K790139.

Who is the listed applicant for MONITOR, OFFICE MODEL 140?

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 MONITOR, OFFICE MODEL 140?

The FDA product code for MONITOR, OFFICE MODEL 140 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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