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FDA 510(k)

TIPOWER POWERDRIVE AND RIMPOWER X & SX

K-Number: K020539 · 2002-06-20

ApplicantTisport
Decision Date2002-06-20
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TIPOWER POWERDRIVE AND RIMPOWER X & SX is the device name listed in this FDA 510(k) record. The listed applicant is Tisport. It received FDA 510(k) clearance on 2002-06-20 under 510(k) number K020539. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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

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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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