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FDA 510(k)

TELEMETRY SYSTEM 315

K-Number: K790144 · 1979-02-23

ApplicantGe Medical Systems Information Technologies
Decision Date1979-02-23
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TELEMETRY SYSTEM 315 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 1979-02-23 under 510(k) number K790144. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELEMETRY SYSTEM 315?

TELEMETRY SYSTEM 315 is a medical device that received FDA 510(k) clearance on 1979-02-23. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K790144.

When did TELEMETRY SYSTEM 315 receive FDA 510(k) clearance?

TELEMETRY SYSTEM 315 received FDA 510(k) clearance on 1979-02-23, under 510(k) number K790144.

Who is the listed applicant for TELEMETRY SYSTEM 315?

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 TELEMETRY SYSTEM 315?

The FDA product code for TELEMETRY SYSTEM 315 is DRG.

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Related Devices (Code: DRG)

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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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