FDA 510(k)

VERTICALIBRE WHEELCHAIR

K-Number: K840626 · 1984-02-27

Decision Date1984-02-27

Product CodeIPL

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

VERTICALIBRE WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Poirier S.A.. It received FDA 510(k) clearance on 1984-02-27 under 510(k) number K840626. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERTICALIBRE WHEELCHAIR?

VERTICALIBRE 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 K840626.

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

VERTICALIBRE WHEELCHAIR received FDA 510(k) clearance on 1984-02-27, under 510(k) number K840626.

Who is the listed applicant for VERTICALIBRE 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 VERTICALIBRE WHEELCHAIR?

The FDA product code for VERTICALIBRE WHEELCHAIR is IPL.

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.

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Other records listing Poirier S.A. as applicant

K840638PORTABLE TRANSIT CHAIR K840639POIRIER COMMODES K840629WHEELCHAIR ACCESSORIES K840630POIRIER REGLADE WHEELCHAIR K840632HEMIPLEGIC WHEELCHAIR K840628LARGE FRONT WHEELS WHEELCHAIR

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Related Devices (Code: IPL)

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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.