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FDA 510(k)

CIE FOLDAWAY WHEELCHAIR

K-Number: K050345 · 2005-03-29

Decision Date2005-03-29
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CIE FOLDAWAY WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Carlsbad International Export, Inc.. It received FDA 510(k) clearance on 2005-03-29 under 510(k) number K050345. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIE FOLDAWAY WHEELCHAIR?

CIE FOLDAWAY WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2005-03-29. The listed applicant is Carlsbad International Export, Inc.. The 510(k) number is K050345.

When did CIE FOLDAWAY WHEELCHAIR receive FDA 510(k) clearance?

CIE FOLDAWAY WHEELCHAIR received FDA 510(k) clearance on 2005-03-29, under 510(k) number K050345.

Who is the listed applicant for CIE FOLDAWAY WHEELCHAIR?

The FDA 510(k) record lists Carlsbad International Export, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CIE FOLDAWAY WHEELCHAIR?

The FDA product code for CIE FOLDAWAY WHEELCHAIR is IOR.

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.

Related Devices (Code: IOR)

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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