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FDA 510(k)

MODEL 9000 BARIATRIC WHEELCHAIR

K-Number: K002317 · 2000-08-25

Decision Date2000-08-25
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL 9000 BARIATRIC 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 2000-08-25 under 510(k) number K002317. 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 9000 BARIATRIC WHEELCHAIR?

MODEL 9000 BARIATRIC WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2000-08-25. The listed applicant is Invacare Corp.. The 510(k) number is K002317.

When did MODEL 9000 BARIATRIC WHEELCHAIR receive FDA 510(k) clearance?

MODEL 9000 BARIATRIC WHEELCHAIR received FDA 510(k) clearance on 2000-08-25, under 510(k) number K002317.

Who is the listed applicant for MODEL 9000 BARIATRIC 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 9000 BARIATRIC WHEELCHAIR?

The FDA product code for MODEL 9000 BARIATRIC 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

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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