FDA 510(k)

POIRIER COMMODES

K-Number: K840639 · 1984-03-09

Decision Date1984-03-09

Product Code

DecisionSubstantially Equivalent

Device Summary

POIRIER COMMODES 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 1984-03-09 under 510(k) number K840639. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POIRIER COMMODES?

POIRIER COMMODES is a medical device that received FDA 510(k) clearance on 1984-03-09. The listed applicant is Poirier S.A.. The 510(k) number is K840639.

When did POIRIER COMMODES receive FDA 510(k) clearance?

POIRIER COMMODES received FDA 510(k) clearance on 1984-03-09, under 510(k) number K840639.

Who is the listed applicant for POIRIER COMMODES?

The FDA 510(k) record lists Poirier S.A. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Poirier S.A. as applicant

K840638PORTABLE TRANSIT CHAIR K840627AMPUTEE WHEELCHAIR K840630POIRIER REGLADE WHEELCHAIR K840629WHEELCHAIR ACCESSORIES K840632HEMIPLEGIC WHEELCHAIR K840628LARGE FRONT WHEELS WHEELCHAIR

View all 17 devices →

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.