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 |