510(k) K142300 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
Arrow GPSCath Balloon Dialation Catheter (150 cm)
| Applicant | Hotspur Technologies, Inc.,, Mountain View CA, US |
| Decision | Substantially Equivalent, Sep 17, 2014 |
| Received | Aug 18, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K142300
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.