Permobil AB
Permobil AB holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2020, with 3 FDA device recalls on record.
Top product codes for Permobil AB
FDA recalls by Permobil AB
- Z-3178-2018 — Permobil powered wheelchairs, Model Numbers: (a) M300 PS, (b) C300 PS, (c) C350 PS, (d) C500 PS, (e) C400 PS Product Usage: The devices identified are intended to provide outdoor and indoor mobility to persons limited to a seated position that can operate a powered wheelchair.
- Z-0006-2018 — Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
- Z-0005-2018 — Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Permobil AB
- K190682 — Explorer Mini
- K191874 — F5 Corpus VS
- K143180 — F3
- K143014 — F5
- K123290 — M300 & M400
- K103477 — PERMOBIL M300 / M400
- K081964 — K450 POWERED WHEELCHAIR
- K071650 — C350 POWERED WHEELCHAIR
- K041219 — ELECTRO
- K032765 — STREET
- K993406 — TRAX, POWERED WHEELCHAIR, MODEL 308686-00-0
- K991658 — PERMOBIL POWERED WHEELCHAIR 1280
- K960951 — PERMOBIL CHAIRMAN L/CS 8
- K942508 — ROBO
- K902954 — OBER2 MONITOR, EYE MOVEMENT (OPHTHALMIC)
Data sourced from openFDA. This site is unofficial and independent of the FDA.