510(k) K170158 ยท PND Midline Catheter
PowerGlide ST Midline Catheter
| Applicant | C.R. Bard, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Jun 1, 2017 |
| Received | Jan 18, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170158
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 17, 2020 | Becton Dickinson & Company PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length
Catalog Number: ST018101D Terminated |
PND | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.