FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50
K-Number: K063736 · 2007-01-17
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Device Summary
Frequently Asked Questions
What is the FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50?
FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50 is a medical device that received FDA 510(k) clearance on 2007-01-17. The listed applicant is Pdg Product Design Group, Inc.. The 510(k) number is K063736.
When did FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50 receive FDA 510(k) clearance?
FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50 received FDA 510(k) clearance on 2007-01-17, under 510(k) number K063736.
Who is the listed applicant for FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50?
The FDA 510(k) record lists Pdg Product Design Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50?
The FDA product code for FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50 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 Pdg Product Design Group, 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
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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