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FDA 510(k)

HEMIPLEGIC WHEELCHAIR

K-Number: K840632 · 1984-02-27

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

Device Summary

HEMIPLEGIC 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 K840632. The device is classified under product code IQC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMIPLEGIC WHEELCHAIR?

HEMIPLEGIC 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 K840632.

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

HEMIPLEGIC WHEELCHAIR received FDA 510(k) clearance on 1984-02-27, under 510(k) number K840632.

Who is the listed applicant for HEMIPLEGIC 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 HEMIPLEGIC WHEELCHAIR?

The FDA product code for HEMIPLEGIC 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.

View all 17 devices →

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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