FDA 510(k)

RADIOTHERAPY TREATMENT

K-Number: K790134 · 1979-02-21

Decision Date1979-02-21

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

RADIOTHERAPY TREATMENT 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 1979-02-21 under 510(k) number K790134. 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 RADIOTHERAPY TREATMENT?

RADIOTHERAPY TREATMENT is a medical device that received FDA 510(k) clearance on 1979-02-21. The listed applicant is General Electric Co.. The 510(k) number is K790134.

When did RADIOTHERAPY TREATMENT receive FDA 510(k) clearance?

RADIOTHERAPY TREATMENT received FDA 510(k) clearance on 1979-02-21, under 510(k) number K790134.

Who is the listed applicant for RADIOTHERAPY TREATMENT?

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 RADIOTHERAPY TREATMENT?

The FDA product code for RADIOTHERAPY TREATMENT is 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.