FDA 510(k) Applications for Medical Device Product Code "KGB"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K970688 | CHEEN HOUNG ENT. CO. LTD. | POCKET RESCUE | 09/26/1997 |
K960401 | HANS RUDOLPH, INC. | ULTIMATE SEAL | 06/20/1996 |