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FDA 510(k)

RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR

K-Number: K981672 · 1998-07-17

ApplicantRadiotherapeutics Corp.
Decision Date1998-07-17
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Radiotherapeutics Corp.. It received FDA 510(k) clearance on 1998-07-17 under 510(k) number K981672. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR?

RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR is a medical device that received FDA 510(k) clearance on 1998-07-17. The listed applicant is Radiotherapeutics Corp.. The 510(k) number is K981672.

When did RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR receive FDA 510(k) clearance?

RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR received FDA 510(k) clearance on 1998-07-17, under 510(k) number K981672.

Who is the listed applicant for RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR?

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

What is the FDA product code for RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR?

The FDA product code for RADIOTHERAPEUTICS RF-2000 RADIOFREQUENCY GENERATOR is GEI.

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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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