510(k) K072311 ยท IOR Wheelchair, Mechanical
TILITE AERO X
| Applicant | Tisport, LLC, Kennewick WA, US |
| Decision | Substantially Equivalent, Sep 21, 2007 |
| Received | Aug 17, 2007 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K072311
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 11, 2018 | TiSport, Llc TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the TiLite wheelchair (anti-tip extension for manual wheelchairs).
Product Usage:
The Terminated |
IOR | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.