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FDA 510(k) Applications for Medical Device Product Code "MZW"
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| 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 |