The following data is part of a premarket notification filed by Biotronik, Inc. with the FDA for Scoutpro Acs.
| Device ID | K101776 |
| 510k Number | K101776 |
| Device Name: | SCOUTPRO ACS |
| 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 |
| Subsequent Product Code | DQX |
| Subsequent Product Code | DRE |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-06-25 |
| Decision Date | 2010-07-23 |