The following data is part of a premarket notification filed by Quinton, Inc. with the FDA for Triple Lumen Right Atrial Catheter.
| Device ID | K852815 |
| 510k Number | K852815 |
| Device Name: | TRIPLE LUMEN RIGHT ATRIAL CATHETER |
| Classification | Catheter, Percutaneous |
| Applicant | QUINTON, INC. 2121 TERRY AVE. Seatle, WA 98121 |
| Contact | Don L Andersen |
| Correspondent | Don L Andersen QUINTON, INC. 2121 TERRY AVE. Seatle, WA 98121 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-07-02 |
| Decision Date | 1985-08-26 |