FDA 510(k) Applications for Medical Device Product Code "KDH"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K981286 | ARMM, INC. | SUPERFLOW IRRIGATION AND ASPIRATION TUBING SETS | 06/19/1998 |
K971259 | B. BRAUN MEDICAL, INC. | COMBIPORT FLUID LAVAGE DEVICE | 10/27/1997 |
K962850 | ETHOX CORP. | TUM-E-VAC | 02/21/1997 |
K983624 | GILTECH PLUS, INC. | GILTECH PLUS CONNECTING TUBE SET | 03/18/1999 |