The following data is part of a premarket notification filed by Biotronik, Inc. with the FDA for Selectra Catheters, Selectra Accessory Kit.
| Device ID | K183265 |
| 510k Number | K183265 |
| Device Name: | Selectra Catheters, Selectra Accessory Kit |
| Classification | Catheter, Percutaneous |
| Applicant | Biotronik, Inc. 6024 Jean Road Lake Oswego, OR 97035 |
| Contact | Jon Brumbaugh |
| Correspondent | Jon Brumbaugh Biotronik, Inc. 6024 Jean Road Lake Oswego, OR 97035 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-11-23 |
| Decision Date | 2018-12-13 |
| Summary: | summary |