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FDA 510(k)

RITA STARBURST XLI ELECTROSURGICAL DEVICE

K-Number: K010060 · 2001-01-23

Decision Date2001-01-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RITA STARBURST XLI ELECTROSURGICAL DEVICE 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 2001-01-23 under 510(k) number K010060. 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 STARBURST XLI ELECTROSURGICAL DEVICE?

RITA STARBURST XLI ELECTROSURGICAL DEVICE is a medical device that received FDA 510(k) clearance on 2001-01-23. The listed applicant is Rita Medical Systems. The 510(k) number is K010060.

When did RITA STARBURST XLI ELECTROSURGICAL DEVICE receive FDA 510(k) clearance?

RITA STARBURST XLI ELECTROSURGICAL DEVICE received FDA 510(k) clearance on 2001-01-23, under 510(k) number K010060.

Who is the listed applicant for RITA STARBURST XLI ELECTROSURGICAL DEVICE?

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 STARBURST XLI ELECTROSURGICAL DEVICE?

The FDA product code for RITA STARBURST XLI ELECTROSURGICAL DEVICE 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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