FDA 510(k)

RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR

K-Number: K032149 · 2003-09-09

Decision Date2003-09-09

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Rita Medical Systems, Inc.. It received FDA 510(k) clearance on 2003-09-09 under 510(k) number K032149. 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 RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR?

RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR is a medical device that received FDA 510(k) clearance on 2003-09-09. The listed applicant is Rita Medical Systems, Inc.. The 510(k) number is K032149.

When did RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR receive FDA 510(k) clearance?

RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR received FDA 510(k) clearance on 2003-09-09, under 510(k) number K032149.

Who is the listed applicant for RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR?

The FDA 510(k) record lists Rita Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR?

The FDA product code for RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR 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.