510(k) K071650 ยท ITI Wheelchair, Powered
C350 POWERED WHEELCHAIR
| Applicant | Permobil AB, Timra, SE |
| Decision | Substantially Equivalent, Sep 12, 2007 |
| Received | Jun 18, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071650
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 15, 2018 | Permobil, Ab 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 Terminated |
ITI | None listed |
| Oct 3, 2017 | Permobil, Ab 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 Terminated |
ITI | None listed |
| Oct 3, 2017 | Permobil, Ab Electric Wheelchair bases:
a) C300
b) C350
c) C400
d) C500 Terminated |
ITI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.