FDA 510(k) Applications for Medical Device Product Code "MZW"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K991923 | CLOSURE MEDICAL CORP. | SOOTHE-N-SEAL CANKER SORE RELIEF | 09/02/1999 |
K073209 | KERR CORPORATION | MAXCEM 2 | 01/29/2008 |