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FDA 510(k)

SENOGRAPHE DMR/SMR/DM

K-Number: K913418 · 1992-01-06

ApplicantGeneral Electric Co.
Decision Date1992-01-06
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SENOGRAPHE DMR/SMR/DM 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 1992-01-06 under 510(k) number K913418. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENOGRAPHE DMR/SMR/DM?

SENOGRAPHE DMR/SMR/DM is a medical device that received FDA 510(k) clearance on 1992-01-06. The listed applicant is General Electric Co.. The 510(k) number is K913418.

When did SENOGRAPHE DMR/SMR/DM receive FDA 510(k) clearance?

SENOGRAPHE DMR/SMR/DM received FDA 510(k) clearance on 1992-01-06, under 510(k) number K913418.

Who is the listed applicant for SENOGRAPHE DMR/SMR/DM?

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 SENOGRAPHE DMR/SMR/DM?

The FDA product code for SENOGRAPHE DMR/SMR/DM is IZH.

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Related Devices (Code: IZH)

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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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