The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Vida Ptv Dilataton Catheter.
| Device ID | K131002 |
| 510k Number | K131002 |
| Device Name: | VIDA PTV DILATATON CATHETER |
| Classification | Pulmonary (pulmonic) Valvuloplasty Catheters/percutaneous Valvuloplasty Catheter |
| Applicant | C.R. BARD, INC. 1625 WEST 3RD ST. Tempe, AZ 85281 -1740 |
| Contact | Aaron Conovaloff |
| Correspondent | Aaron Conovaloff C.R. BARD, INC. 1625 WEST 3RD ST. Tempe, AZ 85281 -1740 |
| Product Code | OMZ |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-04-10 |
| Decision Date | 2013-07-02 |
| Summary: | summary |