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FDA 510(k)

MODEL TOP END TERMINATOR TITANIUM MANUAL WHEELCHAIR

K-Number: K012167 · 2001-08-01

Decision Date2001-08-01
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL TOP END TERMINATOR TITANIUM MANUAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 2001-08-01 under 510(k) number K012167. 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 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.

View all 111 devices →

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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