Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MR COMPATIBLE RITA MODEL 90 ELECTOSURGICAL ACCESSORY

K-Number: K023846 · 2002-12-06

Decision Date2002-12-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MR COMPATIBLE RITA MODEL 90 ELECTOSURGICAL ACCESSORY 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 2002-12-06 under 510(k) number K023846. 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 MR COMPATIBLE RITA MODEL 90 ELECTOSURGICAL ACCESSORY?

MR COMPATIBLE RITA MODEL 90 ELECTOSURGICAL ACCESSORY is a medical device that received FDA 510(k) clearance on 2002-12-06. The listed applicant is Rita Medical Systems. The 510(k) number is K023846.

When did MR COMPATIBLE RITA MODEL 90 ELECTOSURGICAL ACCESSORY receive FDA 510(k) clearance?

MR COMPATIBLE RITA MODEL 90 ELECTOSURGICAL ACCESSORY received FDA 510(k) clearance on 2002-12-06, under 510(k) number K023846.

Who is the listed applicant for MR COMPATIBLE RITA MODEL 90 ELECTOSURGICAL ACCESSORY?

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 MR COMPATIBLE RITA MODEL 90 ELECTOSURGICAL ACCESSORY?

The FDA product code for MR COMPATIBLE RITA MODEL 90 ELECTOSURGICAL ACCESSORY is GEI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Rita Medical Systems as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 11 devices →

Related Devices (Code: GEI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

↑