FDA 510(k) Applications for Medical Device Product Code "KDQ"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K984496 | ATRIUM MEDICAL CORP. | ATRIUM MEDICAL CORPORATION EXPRESS CHEST DRAIN | 05/05/1999 |
K081718 | ATRIUM MEDICAL CORP. | EXPRESS CHEST DRAIN | 07/25/2008 |
K043582 | ATRIUM MEDICAL CORP. | OCEAN CHEST DRAIN | 01/21/2005 |
K962856 | DEKNATEL, INC. | PLEUR-EVAC SAHARA ADULT/PEDIATRIC CHEST DRAINAGE SYSTEM MODEL S-1100, S-1200, 2-2100, AND S-2200 WITH MODEL S-100 AUTOTR | 08/28/1996 |
K062302 | MILLICORE AB | MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM | 10/06/2006 |
K961287 | ROCKET MEDICAL PLC | ROCKET PLEURASEAL II CHEST DRAINAGE SYSTEM | 07/26/1996 |
K962168 | SAGE PRODUCTS, INC. | MUCUS SPECIMEN TRAP | 07/22/1996 |