FDA 510(k)

GENERATOR

K-Number: K772143 · 1978-01-10

ApplicantElectric Field Technology Corp.

Decision Date1978-01-10

Product Code

DecisionSubstantially Equivalent

Device Summary

GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Electric Field Technology Corp.. It received FDA 510(k) clearance on 1978-01-10 under 510(k) number K772143. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERATOR?

GENERATOR is a medical device that received FDA 510(k) clearance on 1978-01-10. The listed applicant is Electric Field Technology Corp.. The 510(k) number is K772143.

When did GENERATOR receive FDA 510(k) clearance?

GENERATOR received FDA 510(k) clearance on 1978-01-10, under 510(k) number K772143.

Who is the listed applicant for GENERATOR?

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

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Related PubMed Literature

PMID: 42547906Image-based evaluation of a commercial AI synthetic CT generator for brain and prostate MR-only radiotherapy.Journal of applied clinical medical physics ()

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.