The following data is part of a premarket notification filed by Covidien with the FDA for Mahurkar Elite Acute Dual Lumen Catheter, Elite Acute Triple Lumen Catheter.
Device ID | K120674 |
510k Number | K120674 |
Device Name: | MAHURKAR ELITE ACUTE DUAL LUMEN CATHETER, ELITE ACUTE TRIPLE LUMEN CATHETER |
Classification | Catheter, Hemodialysis, Non-implanted |
Applicant | COVIDIEN 15 HAMPSHIRE STREET Mansfield, MA 02048 |
Contact | Wing Ng |
Correspondent | Wing Ng COVIDIEN 15 HAMPSHIRE STREET Mansfield, MA 02048 |
Product Code | MPB |
CFR Regulation Number | 876.5540 [🔎] |
Decision | Substantially Equivalent - Kit (SESK) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-03-05 |
Decision Date | 2012-04-04 |
Summary: | summary |