DUET BICYCLE/WHEELCHAIR
K-Number: K913759 · 1991-10-24
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Device Summary
Frequently Asked Questions
What is the DUET BICYCLE/WHEELCHAIR?
DUET BICYCLE/WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1991-10-24. The listed applicant is Robert Hoening Mobility Systems, Inc.. The 510(k) number is K913759.
When did DUET BICYCLE/WHEELCHAIR receive FDA 510(k) clearance?
DUET BICYCLE/WHEELCHAIR received FDA 510(k) clearance on 1991-10-24, under 510(k) number K913759.
Who is the listed applicant for DUET BICYCLE/WHEELCHAIR?
The FDA 510(k) record lists Robert Hoening Mobility Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUET BICYCLE/WHEELCHAIR?
The FDA product code for DUET BICYCLE/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
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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