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FDA 510(k)

G.E. TELEMETRY MONITORING

K-Number: K761259 · 1976-12-21

ApplicantGeneral Electric Co.
Decision Date1976-12-21
Product CodeGYE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

G.E. TELEMETRY MONITORING is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1976-12-21 under 510(k) number K761259. The device is classified under product code GYE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G.E. TELEMETRY MONITORING?

G.E. TELEMETRY MONITORING is a medical device that received FDA 510(k) clearance on 1976-12-21. The listed applicant is General Electric Co.. The 510(k) number is K761259.

When did G.E. TELEMETRY MONITORING receive FDA 510(k) clearance?

G.E. TELEMETRY MONITORING received FDA 510(k) clearance on 1976-12-21, under 510(k) number K761259.

Who is the listed applicant for G.E. TELEMETRY MONITORING?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for G.E. TELEMETRY MONITORING?

The FDA product code for G.E. TELEMETRY MONITORING is GYE.

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Related Devices (Code: GYE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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