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FDA 510(k)

TIPOWER TR RIMPOWER AND TIPOWER TRA RIMPOWER

K-Number: K020639 · 2002-06-20

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

Device Summary

TIPOWER TR RIMPOWER AND TIPOWER TRA RIMPOWER 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 K020639. 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 TR RIMPOWER AND TIPOWER TRA RIMPOWER?

TIPOWER TR RIMPOWER AND TIPOWER TRA RIMPOWER is a medical device that received FDA 510(k) clearance on 2002-06-20. The listed applicant is Tisport. The 510(k) number is K020639.

When did TIPOWER TR RIMPOWER AND TIPOWER TRA RIMPOWER receive FDA 510(k) clearance?

TIPOWER TR RIMPOWER AND TIPOWER TRA RIMPOWER received FDA 510(k) clearance on 2002-06-20, under 510(k) number K020639.

Who is the listed applicant for TIPOWER TR RIMPOWER AND TIPOWER TRA RIMPOWER?

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 TR RIMPOWER AND TIPOWER TRA RIMPOWER?

The FDA product code for TIPOWER TR RIMPOWER AND TIPOWER TRA RIMPOWER is ITI.

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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.

K023606TILITE YG AND TILITE YGSK020539TIPOWER POWERDRIVE AND RIMPOWER X & SXK990555TISPORT X AND TISPORT XCK990358CROSS SPORT, RIGID WHEELCHAIR

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.

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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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