The following data is part of a premarket notification filed by Covidien Llc with the FDA for Fortrex 0.035 Otw Pta Balloon Catheter.
| Device ID | K142654 |
| 510k Number | K142654 |
| Device Name: | Fortrex 0.035 OTW PTA Balloon Catheter |
| Classification | Catheter, Angioplasty, Peripheral, Transluminal |
| Applicant | Covidien LLC 3033 Campus Drive Plymouth, MN 55441 |
| Contact | Rupali Gupta |
| Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| Product Code | LIT |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2014-09-18 |
| Decision Date | 2014-10-28 |
| Summary: | summary |