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FDA 510(k)

NISSIN PEDIATRIC SERIES WHEELCHAIR

K-Number: K063521 · 2007-02-05

Decision Date2007-02-05
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NISSIN PEDIATRIC SERIES WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Nissin Medical, Inc.. It received FDA 510(k) clearance on 2007-02-05 under 510(k) number K063521. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NISSIN PEDIATRIC SERIES WHEELCHAIR?

NISSIN PEDIATRIC SERIES WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2007-02-05. The listed applicant is Nissin Medical, Inc.. The 510(k) number is K063521.

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

NISSIN PEDIATRIC SERIES WHEELCHAIR received FDA 510(k) clearance on 2007-02-05, under 510(k) number K063521.

Who is the listed applicant for NISSIN PEDIATRIC SERIES WHEELCHAIR?

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

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

The FDA product code for NISSIN PEDIATRIC SERIES WHEELCHAIR is INM.

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: INM)

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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