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FDA 510(k)

ALT WHEELCHAIR

K-Number: K864573 · 1986-12-16

ApplicantAlt Design
Decision Date1986-12-16
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ALT WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Alt Design. It received FDA 510(k) clearance on 1986-12-16 under 510(k) number K864573. 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 ALT WHEELCHAIR?

ALT WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1986-12-16. The listed applicant is Alt Design. The 510(k) number is K864573.

When did ALT WHEELCHAIR receive FDA 510(k) clearance?

ALT WHEELCHAIR received FDA 510(k) clearance on 1986-12-16, under 510(k) number K864573.

Who is the listed applicant for ALT WHEELCHAIR?

The FDA 510(k) record lists Alt Design as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALT WHEELCHAIR?

The FDA product code for ALT 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.

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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