FDA 510(k)

RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90

K-Number: K992693 · 1999-09-10

Decision Date1999-09-10

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90 is the device name listed in this FDA 510(k) record. The listed applicant is Rita Medical Systems. It received FDA 510(k) clearance on 1999-09-10 under 510(k) number K992693. 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 90 ELECTROSURGICAL ACCESSORY, MODEL 90?

RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90 is a medical device that received FDA 510(k) clearance on 1999-09-10. The listed applicant is Rita Medical Systems. The 510(k) number is K992693.

When did RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90 receive FDA 510(k) clearance?

RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90 received FDA 510(k) clearance on 1999-09-10, under 510(k) number K992693.

Who is the listed applicant for RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90?

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

What is the FDA product code for RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90?

The FDA product code for RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90 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.