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FDA 510(k)

WIZARD PEDIATRIC WHEELCHAIR

K-Number: K934560 · 1994-01-07

Decision Date1994-01-07
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WIZARD PEDIATRIC WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Snug Seat, Inc.. It received FDA 510(k) clearance on 1994-01-07 under 510(k) number K934560. 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 WIZARD PEDIATRIC WHEELCHAIR?

WIZARD PEDIATRIC WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Snug Seat, Inc.. The 510(k) number is K934560.

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

WIZARD PEDIATRIC WHEELCHAIR received FDA 510(k) clearance on 1994-01-07, under 510(k) number K934560.

Who is the listed applicant for WIZARD PEDIATRIC WHEELCHAIR?

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

What is the FDA product code for WIZARD PEDIATRIC WHEELCHAIR?

The FDA product code for WIZARD PEDIATRIC 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.

Other records listing Snug Seat, Inc. as applicant

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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