The following data is part of a premarket notification filed by Sequent Medical, Inc with the FDA for Via Microcatheter, Via Plus Microcatheter.
| Device ID | K132652 |
| 510k Number | K132652 |
| Device Name: | VIA MICROCATHETER, VIA PLUS MICROCATHETER |
| Classification | Catheter, Percutaneous |
| Applicant | SEQUENT MEDICAL, INC 11A COLUMBIA Aliso Viejo, CA 92656 |
| Contact | Melanie Parravi |
| Correspondent | Melanie Parravi SEQUENT MEDICAL, INC 11A COLUMBIA Aliso Viejo, CA 92656 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-08-26 |
| Decision Date | 2013-12-20 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00851566003703 | K132652 | 000 |
| 00851566003420 | K132652 | 000 |