The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Sidekick And Usher Support Catheters.
| Device ID | K131493 |
| 510k Number | K131493 |
| Device Name: | SIDEKICK AND USHER SUPPORT CATHETERS |
| Classification | Catheter, Percutaneous |
| Applicant | C.R. BARD, INC. 1625 WEST 3RD ST. Tempe, AZ 85281 -1740 |
| Contact | Timothy Wade |
| Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2013-05-23 |
| Decision Date | 2013-08-02 |
| Summary: | summary |