The following data is part of a premarket notification filed by Catheter Innovations, Inc. with the FDA for Dual Lumen Midline Catheter.
| Device ID | K010349 |
| 510k Number | K010349 |
| Device Name: | DUAL LUMEN MIDLINE CATHETER |
| Classification | Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days |
| Applicant | CATHETER INNOVATIONS, INC. 3598 WEST 1820 SOUTH Salt Lake City, UT 84104 |
| Contact | Roger L Richins |
| Correspondent | Roger L Richins CATHETER INNOVATIONS, INC. 3598 WEST 1820 SOUTH Salt Lake City, UT 84104 |
| Product Code | LJS |
| CFR Regulation Number | 880.5970 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-02-05 |
| Decision Date | 2001-02-28 |