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FDA 510(k)

POSITELEC WHEELCHAIR

K-Number: K840640 · 1984-02-27

ApplicantPoirier S.A.
Decision Date1984-02-27
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POSITELEC 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 K840640. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POSITELEC WHEELCHAIR?

POSITELEC 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 K840640.

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

POSITELEC WHEELCHAIR received FDA 510(k) clearance on 1984-02-27, under 510(k) number K840640.

Who is the listed applicant for POSITELEC 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 POSITELEC WHEELCHAIR?

The FDA product code for POSITELEC WHEELCHAIR is ITI.

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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

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.

K840638PORTABLE TRANSIT CHAIRK840639POIRIER COMMODESK840629WHEELCHAIR ACCESSORIESK840630POIRIER REGLADE WHEELCHAIRK840632HEMIPLEGIC WHEELCHAIRK840628LARGE FRONT WHEELS WHEELCHAIR

View all 17 devices →

Related Devices (Code: ITI)

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.

K262582Electric wheelchair (GP100)Suzhou Green Pine Medical Co., Ltd.K262054Electric WheelchairYongkang Joymax Medical Technology Co., Ltd.K260053Power Wheelchair (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229Electric wheelchair (HC819N, HC830N, HC831N)Yongkang Hengyi Vehicle Co., Ltd.K261354Electric wheelchair (D03)Foshan Sowell Medical Technology Co., Ltd.K261149Electric Wheelchair (DY611A-2, DY612A-1)Zhejiang Lumbre Electric Appliance Co., Ltd.

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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