FDA 510(k) Applications for Medical Device Product Code "EGM"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K962017 | AMERICAN JET INJECTOR CORP. | HYPODERMIC JET INJECTION APPARATUS | 07/26/1996 |
K964802 | INTRA VANTAGE, INC. | CYBERJET LOCAL ANESTHESIA SYSTEM | 05/27/1997 |
K083811 | W & H DENTALWERK BUERMOOS GMBH | W&H HANDPIECE ANESTO, MODEL: RA-5 | 01/14/2010 |