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FDA 510(k)

STORM TDX POWER WHEELCHAIR

K-Number: K023589 · 2002-11-19

ApplicantInvacare Corp.
Decision Date2002-11-19
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STORM TDX POWER WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 2002-11-19 under 510(k) number K023589. 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 STORM TDX POWER WHEELCHAIR?

STORM TDX POWER WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2002-11-19. The listed applicant is Invacare Corp.. The 510(k) number is K023589.

When did STORM TDX POWER WHEELCHAIR receive FDA 510(k) clearance?

STORM TDX POWER WHEELCHAIR received FDA 510(k) clearance on 2002-11-19, under 510(k) number K023589.

Who is the listed applicant for STORM TDX POWER WHEELCHAIR?

The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STORM TDX POWER WHEELCHAIR?

The FDA product code for STORM TDX POWER WHEELCHAIR is ITI.

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Other records listing Invacare Corp. as applicant

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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

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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