FDA 510(k) Applications for Medical Device Product Code "JQF"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K051111 | SENTINEL CH. SRL | SENTINEL UIBC LIQUID | 11/17/2005 |
K984122 | WAKO CHEMICALS, USA, INC. | WAKO L-TYPE UIBC, WAKO UIBC CALIBRATOR | 01/20/1999 |