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FDA 510(k)

RITA RF GENERATOR AND ACCESSORIES, MODEL 500 SERIES

K-Number: K983214 · 2000-03-27

ApplicantRita Medical Systems
Decision Date2000-03-27
Product CodeGXD
Advisory CommitteeNE
DecisionUnknown

Device Summary

RITA RF GENERATOR AND ACCESSORIES, MODEL 500 SERIES 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 2000-03-27 under 510(k) number K983214. The device is classified under product code GXD. It was reviewed by the NE advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the RITA RF GENERATOR AND ACCESSORIES, MODEL 500 SERIES?

RITA RF GENERATOR AND ACCESSORIES, MODEL 500 SERIES is a medical device that received FDA 510(k) clearance on 2000-03-27. The listed applicant is Rita Medical Systems. The 510(k) number is K983214.

When did RITA RF GENERATOR AND ACCESSORIES, MODEL 500 SERIES receive FDA 510(k) clearance?

RITA RF GENERATOR AND ACCESSORIES, MODEL 500 SERIES received FDA 510(k) clearance on 2000-03-27, under 510(k) number K983214.

Who is the listed applicant for RITA RF GENERATOR AND ACCESSORIES, MODEL 500 SERIES?

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 RF GENERATOR AND ACCESSORIES, MODEL 500 SERIES?

The FDA product code for RITA RF GENERATOR AND ACCESSORIES, MODEL 500 SERIES is GXD.

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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.

K062935HABIB 4X LAPAROSCOPICK040989RITA SYSTEMSK030967RITA STARBURST SDE ELECTROSURGICAL DEVICEK023846MR COMPATIBLE RITA MODEL 90 ELECTOSURGICAL ACCESSORYK021329RITA SYSTEMK003676RITA MODEL 2500 ELECTROSURGICAL RF GENERATOR

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Related Devices (Code: GXD)

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.

K251247GX1 Radiofrequency Generator Kit (RFG-X1-120V); GX1 Radiofrequency Generator Kit (RFG-X1-220V); GX1 Radiofrequency Generator Kit (RFG-X1-240V); GX1 System Release Rest of World (GX1-SYS-ROW); GX1 Radiofrequency Generator (51779845-01); GX1 Radiofrequency Generator (51779845-02); GX1 Radiofrequency Generator (51779845-03)Boston Scientific Neuromodulation CorporationK242057COOLIEF* Radiofrequency Generator (CRG-BASIC, CRG-BASIC-R, CRG-ADVANCED, CRG-ADVANCED-R)Avanos Medical, Inc.K232632Racz Neurostat RF GeneratorEpimed InternationalK231675OneRF Ablation SystemNeuroone Medical Technologies Corp.K220122APEX 6Rf Innovations, Inc.K203293Abbott Medical Grounding Pad, model RF-DGP-ISABBOTT MEDICAL

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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