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FDA 510(k)

RADVIEW IMAGER SYSTEM

K-Number: K790942 · 1979-06-27

ApplicantGeneral Electric Co.
Decision Date1979-06-27
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADVIEW IMAGER SYSTEM 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 1979-06-27 under 510(k) number K790942. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADVIEW IMAGER SYSTEM?

RADVIEW IMAGER SYSTEM is a medical device that received FDA 510(k) clearance on 1979-06-27. The listed applicant is General Electric Co.. The 510(k) number is K790942.

When did RADVIEW IMAGER SYSTEM receive FDA 510(k) clearance?

RADVIEW IMAGER SYSTEM received FDA 510(k) clearance on 1979-06-27, under 510(k) number K790942.

Who is the listed applicant for RADVIEW IMAGER SYSTEM?

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 RADVIEW IMAGER SYSTEM?

The FDA product code for RADVIEW IMAGER SYSTEM is JAK.

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Related Devices (Code: JAK)

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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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