The following data is part of a premarket notification filed by Boston Scientific Corporation with the FDA for Mamba And Mamba Flex Microcatheters.
| Device ID | K171452 |
| 510k Number | K171452 |
| Device Name: | MAMBA And MAMBA FLEX Microcatheters |
| Classification | Catheter, Percutaneous |
| Applicant | Boston Scientific Corporation Three Scimed Place Maple Grove, MN 55311 |
| Contact | Sherry Kollmann |
| Correspondent | Sherry Kollmann Boston Scientific Corporation Three Scimed Place Maple Grove, MN 55311 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-05-17 |
| Decision Date | 2017-08-21 |
| Summary: | summary |