POIRIER REGLADE WHEELCHAIR
K-Number: K840630 · 1984-02-27
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Device Summary
Frequently Asked Questions
What is the POIRIER REGLADE WHEELCHAIR?
POIRIER REGLADE WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1984-02-27. The listed applicant is Poirier S.A.. The 510(k) number is K840630.
When did POIRIER REGLADE WHEELCHAIR receive FDA 510(k) clearance?
POIRIER REGLADE WHEELCHAIR received FDA 510(k) clearance on 1984-02-27, under 510(k) number K840630.
Who is the listed applicant for POIRIER REGLADE WHEELCHAIR?
The FDA 510(k) record lists Poirier S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POIRIER REGLADE WHEELCHAIR?
The FDA product code for POIRIER REGLADE WHEELCHAIR is IQC.
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 Poirier S.A. 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: IQC)
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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