The following data is part of a premarket notification filed by Abbott Vascular with the FDA for Mini Trek Rx Coronary Dilatation Catheter (including 1.20 Mm Size), Mini Trek Otw Coronary Dilatation Catheter (includin.
| Device ID | K123279 |
| 510k Number | K123279 |
| Device Name: | MINI TREK RX CORONARY DILATATION CATHETER (INCLUDING 1.20 MM SIZE), MINI TREK OTW CORONARY DILATATION CATHETER (INCLUDIN |
| Classification | Catheters, Transluminal Coronary Angioplasty, Percutaneous |
| Applicant | Abbott Vascular 26531 YNEZ ROAD P.O. BOX 9018 Temecula, CA 92589 -9018 |
| Contact | Suzanne Redman |
| Correspondent | Suzanne Redman Abbott Vascular 26531 YNEZ ROAD P.O. BOX 9018 Temecula, CA 92589 -9018 |
| Product Code | LOX |
| CFR Regulation Number | 870.5100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-10-22 |
| Decision Date | 2013-01-30 |
| Summary: | summary |