The following data is part of a premarket notification filed by Cordis Corporation with the FDA for Saber Percutaneous Transluminal Angioplasty Dilatation Catheter.
| Device ID | K133843 |
| 510k Number | K133843 |
| Device Name: | SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER |
| Classification | Catheter, Angioplasty, Peripheral, Transluminal |
| Applicant | CORDIS CORPORATION 6500 PASEO PADRE PKWY Fremont, CA 94555 |
| Contact | Kim Fonda |
| Correspondent | Kim Fonda CORDIS CORPORATION 6500 PASEO PADRE PKWY Fremont, CA 94555 |
| Product Code | LIT |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-12-18 |
| Decision Date | 2014-06-27 |
| Summary: | summary |