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510(k) K840639

POIRIER COMMODES by Poirier S.A.

K840639 is an FDA 510(k) premarket notification submitted by Poirier S.A. for the device "POIRIER COMMODES". The FDA issued a decision of Substantially Equivalent on Mar 9, 1984. Poirier S.A. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Mar 9, 1984
Date Received
Jan 20, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Poirier S.A.

  • K840638 — PORTABLE TRANSIT CHAIR (Mar 16, 1984)
  • K840632 — HEMIPLEGIC WHEELCHAIR (Feb 27, 1984)
  • K840626 — VERTICALIBRE WHEELCHAIR (Feb 27, 1984)
  • K840634 — OLYMPIC & BASKET WHEELCHAIRS (Feb 27, 1984)
  • K840640 — POSITELEC WHEELCHAIR (Feb 27, 1984)
  • K840628 — LARGE FRONT WHEELS WHEELCHAIR (Feb 27, 1984)
  • K840234 — POIRIER VARIABLE WHEELCHAIR (Feb 27, 1984)
  • K840630 — POIRIER REGLADE WHEELCHAIR (Feb 27, 1984)
  • K840627 — AMPUTEE WHEELCHAIR (Feb 27, 1984)
  • K840631 — ARNAS WHEELCHAIR (Feb 27, 1984)

FDA data resources