POIRIER MANUAL WHEELCHAIR
K-Number: K864790 · 1986-12-17
Advertisement
Device Summary
Frequently Asked Questions
What is the POIRIER MANUAL WHEELCHAIR?
POIRIER MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1986-12-17. The listed applicant is Roseburg SA. The 510(k) number is K864790.
When did POIRIER MANUAL WHEELCHAIR receive FDA 510(k) clearance?
POIRIER MANUAL WHEELCHAIR received FDA 510(k) clearance on 1986-12-17, under 510(k) number K864790.
Who is the listed applicant for POIRIER MANUAL WHEELCHAIR?
The FDA 510(k) record lists Roseburg SA as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POIRIER MANUAL WHEELCHAIR?
The FDA product code for POIRIER MANUAL 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 Roseburg SA 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.
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.
Advertisement