TEH LIN POWERED WHEELCHAIR, MODEL MDG-201
K-Number: K022696 · 2003-02-07
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Device Summary
Frequently Asked Questions
What is the TEH LIN POWERED WHEELCHAIR, MODEL MDG-201?
TEH LIN POWERED WHEELCHAIR, MODEL MDG-201 is a medical device that received FDA 510(k) clearance on 2003-02-07. The listed applicant is Teh Lin Prosthetic & Orthopaedic, Inc.. The 510(k) number is K022696.
When did TEH LIN POWERED WHEELCHAIR, MODEL MDG-201 receive FDA 510(k) clearance?
TEH LIN POWERED WHEELCHAIR, MODEL MDG-201 received FDA 510(k) clearance on 2003-02-07, under 510(k) number K022696.
Who is the listed applicant for TEH LIN POWERED WHEELCHAIR, MODEL MDG-201?
The FDA 510(k) record lists Teh Lin Prosthetic & Orthopaedic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TEH LIN POWERED WHEELCHAIR, MODEL MDG-201?
The FDA product code for TEH LIN POWERED WHEELCHAIR, MODEL MDG-201 is ITI.
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 Teh Lin Prosthetic & Orthopaedic, 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: ITI)
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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