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FDA 510(k)

RADIUS AND SONOCHROME

K-Number: K902070 · 1990-08-28

ApplicantGeneral Electric Co.
Decision Date1990-08-28
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIUS AND SONOCHROME 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 1990-08-28 under 510(k) number K902070. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIUS AND SONOCHROME?

RADIUS AND SONOCHROME is a medical device that received FDA 510(k) clearance on 1990-08-28. The listed applicant is General Electric Co.. The 510(k) number is K902070.

When did RADIUS AND SONOCHROME receive FDA 510(k) clearance?

RADIUS AND SONOCHROME received FDA 510(k) clearance on 1990-08-28, under 510(k) number K902070.

Who is the listed applicant for RADIUS AND SONOCHROME?

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 RADIUS AND SONOCHROME?

The FDA product code for RADIUS AND SONOCHROME is ITX.

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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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