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FDA 510(k)

THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR

K-Number: K990557 · 1999-03-22

Decision Date1999-03-22
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Pdg Product Design Group, Inc.. It received FDA 510(k) clearance on 1999-03-22 under 510(k) number K990557. 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 THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR?

THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1999-03-22. The listed applicant is Pdg Product Design Group, Inc.. The 510(k) number is K990557.

When did THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR receive FDA 510(k) clearance?

THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR received FDA 510(k) clearance on 1999-03-22, under 510(k) number K990557.

Who is the listed applicant for THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR?

The FDA 510(k) record lists Pdg Product Design Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR?

The FDA product code for THE STELLAR TILT, MANUALLY OPERATED 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 Pdg Product Design Group, Inc. 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 7 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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