The following data is part of a premarket notification filed by Lemaitre Vascular, Inc. with the FDA for Unballoon Non-occlusive Modeling Catheter.
| Device ID | K123531 |
| 510k Number | K123531 |
| Device Name: | UNBALLOON NON-OCCLUSIVE MODELING CATHETER |
| Classification | Catheter, Percutaneous |
| Applicant | LEMAITRE VASCULAR, INC. 63 SECOND AVENUE Burlington, MA 01803 |
| Contact | Bryan Cowell, Rac |
| Correspondent | Bryan Cowell, Rac LEMAITRE VASCULAR, INC. 63 SECOND AVENUE Burlington, MA 01803 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-11-16 |
| Decision Date | 2012-12-14 |
| Summary: | summary |