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FDA 510(k)

ARROW FWD POWER WHEELCHAIR

K-Number: K991168 · 1999-06-25

ApplicantInvacare Corp.
Decision Date1999-06-25
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ARROW FWD POWER 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 1999-06-25 under 510(k) number K991168. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARROW FWD POWER WHEELCHAIR?

ARROW FWD POWER WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1999-06-25. The listed applicant is Invacare Corp.. The 510(k) number is K991168.

When did ARROW FWD POWER WHEELCHAIR receive FDA 510(k) clearance?

ARROW FWD POWER WHEELCHAIR received FDA 510(k) clearance on 1999-06-25, under 510(k) number K991168.

Who is the listed applicant for ARROW FWD POWER 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 ARROW FWD POWER WHEELCHAIR?

The FDA product code for ARROW FWD POWER WHEELCHAIR is ITI.

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Other records listing Invacare Corp. as applicant

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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.

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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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