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FDA 510(k)

IGLIDE MANUAL ASSIST WHEELCHAIR

K-Number: K030250 · 2003-03-04

ApplicantIndependence Technology, LLC
Decision Date2003-03-04
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

IGLIDE MANUAL ASSIST WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Independence Technology, LLC. It received FDA 510(k) clearance on 2003-03-04 under 510(k) number K030250. 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 IGLIDE MANUAL ASSIST WHEELCHAIR?

IGLIDE MANUAL ASSIST WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2003-03-04. The listed applicant is Independence Technology, LLC. The 510(k) number is K030250.

When did IGLIDE MANUAL ASSIST WHEELCHAIR receive FDA 510(k) clearance?

IGLIDE MANUAL ASSIST WHEELCHAIR received FDA 510(k) clearance on 2003-03-04, under 510(k) number K030250.

Who is the listed applicant for IGLIDE MANUAL ASSIST WHEELCHAIR?

The FDA 510(k) record lists Independence Technology, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IGLIDE MANUAL ASSIST WHEELCHAIR?

The FDA product code for IGLIDE MANUAL ASSIST WHEELCHAIR is ITI.

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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

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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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