RITA SYSTEM
K-Number: K021329 · 2002-10-09
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Device Summary
Frequently Asked Questions
What is the RITA SYSTEM?
RITA SYSTEM is a medical device that received FDA 510(k) clearance on 2002-10-09. The listed applicant is Rita Medical Systems. The 510(k) number is K021329.
When did RITA SYSTEM receive FDA 510(k) clearance?
RITA SYSTEM received FDA 510(k) clearance on 2002-10-09, under 510(k) number K021329.
Who is the listed applicant for RITA SYSTEM?
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 SYSTEM?
The FDA product code for RITA SYSTEM 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.
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.
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