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FDA 510(k) Applications for Medical Device Product Code "KMK"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K963365 | BYRD MEDICAL DEVICES, INC. | MULTI-PURPOSE MEDICAL TUBE HOLDER | 10/11/1996 |
K180994 | Interrad Medical Inc | SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F | 07/09/2019 |
K981860 | PARAWORKS ENTERPRISE, LTD. | A P HARNESS | 06/03/1999 |