FDA 510(k) Applications for Medical Device Product Code "DWQ"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K212894 | LeMaitre Vascular Inc. | PhasTIPP | 03/31/2022 |
K041453 | SMITH & NEPHEW, INC. | SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023 | 07/22/2004 |
K032387 | SMITH & NEPHEW, INC. | TRIVEX SYSTEM | 10/29/2003 |