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FDA 510(k)

ICON ADULT MANUAL

K-Number: K110985 · 2011-05-03

Decision Date2011-05-03
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ICON ADULT MANUAL is the device name listed in this FDA 510(k) record. The listed applicant is Icon Wheelchairs, Inc.. It received FDA 510(k) clearance on 2011-05-03 under 510(k) number K110985. 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 ICON ADULT MANUAL?

ICON ADULT MANUAL is a medical device that received FDA 510(k) clearance on 2011-05-03. The listed applicant is Icon Wheelchairs, Inc.. The 510(k) number is K110985.

When did ICON ADULT MANUAL receive FDA 510(k) clearance?

ICON ADULT MANUAL received FDA 510(k) clearance on 2011-05-03, under 510(k) number K110985.

Who is the listed applicant for ICON ADULT MANUAL?

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

What is the FDA product code for ICON ADULT MANUAL?

The FDA product code for ICON ADULT MANUAL 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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