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FDA 510(k)

MODEL 410 ALERT AND TELECOMMUNICATION SYSTEM

K-Number: K894958 · 1989-11-03

ApplicantGe Medical Systems Information Technologies
Decision Date1989-11-03
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODEL 410 ALERT AND TELECOMMUNICATION SYSTEM 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 1989-11-03 under 510(k) number K894958. 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 MODEL 410 ALERT AND TELECOMMUNICATION SYSTEM?

MODEL 410 ALERT AND TELECOMMUNICATION SYSTEM is a medical device that received FDA 510(k) clearance on 1989-11-03. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K894958.

When did MODEL 410 ALERT AND TELECOMMUNICATION SYSTEM receive FDA 510(k) clearance?

MODEL 410 ALERT AND TELECOMMUNICATION SYSTEM received FDA 510(k) clearance on 1989-11-03, under 510(k) number K894958.

Who is the listed applicant for MODEL 410 ALERT AND TELECOMMUNICATION SYSTEM?

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 MODEL 410 ALERT AND TELECOMMUNICATION SYSTEM?

The FDA product code for MODEL 410 ALERT AND TELECOMMUNICATION SYSTEM 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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