TIPOWER POWERDRIVE AND RIMPOWER X & SX
K-Number: K020539 · 2002-06-20
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Device Summary
Frequently Asked Questions
What is the TIPOWER POWERDRIVE AND RIMPOWER X & SX?
TIPOWER POWERDRIVE AND RIMPOWER X & SX is a medical device that received FDA 510(k) clearance on 2002-06-20. The listed applicant is Tisport. The 510(k) number is K020539.
When did TIPOWER POWERDRIVE AND RIMPOWER X & SX receive FDA 510(k) clearance?
TIPOWER POWERDRIVE AND RIMPOWER X & SX received FDA 510(k) clearance on 2002-06-20, under 510(k) number K020539.
Who is the listed applicant for TIPOWER POWERDRIVE AND RIMPOWER X & SX?
The FDA 510(k) record lists Tisport as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TIPOWER POWERDRIVE AND RIMPOWER X & SX?
The FDA product code for TIPOWER POWERDRIVE AND RIMPOWER X & SX is ITI.
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 Tisport 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: ITI)
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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