510(k) K062425 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
LIFECATH S PICC AND MIDLINE CATHETER
| Applicant | Vygon Corp., Norristown PA, US |
| Decision | Substantially Equivalent, Sep 15, 2006 |
| Received | Aug 18, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062425
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 29, 2011 | Vygon Corporation LIFECATH S PICC
Catheter, Percutaneous, Intravascular
Product Code 2296.211
Product Usage:: Intravascular catheter Terminated |
LJS | None listed |
| Jun 29, 2011 | Vygon Corporation LIFECATH S PICC with Microflash Introducer
Catheter, Percutaneous, Intravascular
Product Code 2296.214
Product Usage: Intravascular catheter Terminated |
LJS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.