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FDA 510(k)

NISSIN SERIES MECHANICAL WHEELCHAIR

K-Number: K052521 · 2005-09-26

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

Device Summary

NISSIN SERIES MECHANICAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Nissin Medical Industries Co., Ltd.. It received FDA 510(k) clearance on 2005-09-26 under 510(k) number K052521. 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 NISSIN SERIES MECHANICAL WHEELCHAIR?

NISSIN SERIES MECHANICAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2005-09-26. The listed applicant is Nissin Medical Industries Co., Ltd.. The 510(k) number is K052521.

When did NISSIN SERIES MECHANICAL WHEELCHAIR receive FDA 510(k) clearance?

NISSIN SERIES MECHANICAL WHEELCHAIR received FDA 510(k) clearance on 2005-09-26, under 510(k) number K052521.

Who is the listed applicant for NISSIN SERIES MECHANICAL WHEELCHAIR?

The FDA 510(k) record lists Nissin Medical Industries Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NISSIN SERIES MECHANICAL WHEELCHAIR?

The FDA product code for NISSIN SERIES MECHANICAL 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

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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