TREVAIR CHAIR ADULT
K-Number: K102061 · 2010-12-13
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Device Summary
Frequently Asked Questions
What is the TREVAIR CHAIR ADULT?
TREVAIR CHAIR ADULT is a medical device that received FDA 510(k) clearance on 2010-12-13. The listed applicant is Patmont Motor Werks, Inc.. The 510(k) number is K102061.
When did TREVAIR CHAIR ADULT receive FDA 510(k) clearance?
TREVAIR CHAIR ADULT received FDA 510(k) clearance on 2010-12-13, under 510(k) number K102061.
Who is the listed applicant for TREVAIR CHAIR ADULT?
The FDA 510(k) record lists Patmont Motor Werks, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TREVAIR CHAIR ADULT?
The FDA product code for TREVAIR CHAIR ADULT 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 Patmont Motor Werks, 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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