MODEL TOP END TERMINATOR TITANIUM MANUAL WHEELCHAIR
K-Number: K012167 · 2001-08-01
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Device Summary
Frequently Asked Questions
What is the MODEL TOP END TERMINATOR TITANIUM MANUAL WHEELCHAIR?
MODEL TOP END TERMINATOR TITANIUM MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2001-08-01. The listed applicant is Invacare Corp.. The 510(k) number is K012167.
When did MODEL TOP END TERMINATOR TITANIUM MANUAL WHEELCHAIR receive FDA 510(k) clearance?
MODEL TOP END TERMINATOR TITANIUM MANUAL WHEELCHAIR received FDA 510(k) clearance on 2001-08-01, under 510(k) number K012167.
Who is the listed applicant for MODEL TOP END TERMINATOR TITANIUM MANUAL WHEELCHAIR?
The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL TOP END TERMINATOR TITANIUM MANUAL WHEELCHAIR?
The FDA product code for MODEL TOP END TERMINATOR TITANIUM MANUAL 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 Invacare Corp. 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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