The following data is part of a premarket notification filed by Biotronik, Inc. with the FDA for Selectra 7f Catheters.
| Device ID | K123324 |
| 510k Number | K123324 |
| Device Name: | SELECTRA 7F CATHETERS |
| 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 | 2012-10-26 |
| Decision Date | 2013-01-11 |
| Summary: | summary |