FDA 510(k) Applications for Medical Device Product Code "CAN"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K162811 | Essex Industries, Inc. | MR Conditional CGA 870 | 03/02/2017 |
K060265 | REMCORE, INC. | REMCORE REMOTE CONTROLLED OXYGEN REGULATOR | 10/25/2006 |
K061785 | RESPONSIVE RESPIRATORY INC. | CYL-FIL OXYGEN SYSTEM | 09/07/2006 |
K080243 | SAN CHEONG CO. LTD. | PORTABLE OXYGEN UNIT SCA900 | 04/07/2009 |