FDA 510(k)

RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000

K-Number: K955144 · 1996-04-07

Decision Date1996-04-07

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Radiotherapeutics Corp.. It received FDA 510(k) clearance on 1996-04-07 under 510(k) number K955144. 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 GENERATOR MODEL RF-1000?

RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000 is a medical device that received FDA 510(k) clearance on 1996-04-07. The listed applicant is Radiotherapeutics Corp.. The 510(k) number is K955144.

When did RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000 receive FDA 510(k) clearance?

RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000 received FDA 510(k) clearance on 1996-04-07, under 510(k) number K955144.

Who is the listed applicant for RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000?

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 GENERATOR MODEL RF-1000?

The FDA product code for RADIOTHERAPEUTICS RF GENERATOR MODEL RF-1000 is GEI.

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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.