FDA 510(k) Applications Submitted by Cerenovus, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K221930 | 07/01/2022 | CEREGLIDE 71 Intermediate Catheter | Cerenovus, Inc. |
| K221934 | 07/01/2022 | CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set | Cerenovus, Inc. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact