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FDA 510(k)

SYRYKER SORANO WHEELCHAIR

K-Number: K051369 · 2005-09-26

Decision Date2005-09-26
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SYRYKER SORANO WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Canada. It received FDA 510(k) clearance on 2005-09-26 under 510(k) number K051369. 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 SYRYKER SORANO WHEELCHAIR?

SYRYKER SORANO WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2005-09-26. The listed applicant is Stryker Canada. The 510(k) number is K051369.

When did SYRYKER SORANO WHEELCHAIR receive FDA 510(k) clearance?

SYRYKER SORANO WHEELCHAIR received FDA 510(k) clearance on 2005-09-26, under 510(k) number K051369.

Who is the listed applicant for SYRYKER SORANO WHEELCHAIR?

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

What is the FDA product code for SYRYKER SORANO WHEELCHAIR?

The FDA product code for SYRYKER SORANO 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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