FDA 510(k) Applications for Medical Device Product Code "CJO"
(Alpha-Naphthyl Phosphate, Alkaline Phosphatase Or Isoenzymes)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K982328 | BAYER CORP. | BAYER ADVIA IMS SYSTEM (IN VITRO DIAGNOSTIC SYSTEM) | 01/29/1999 |
| K121907 | SIEMENS HEALTHCARE DIAGNOSTICS | DIMENSION ALKALINE PHOSPHATASE FLEX REAGENT CARTRIDGE, DIMENSION ALKALINE PHOSPHATASE CALIBRATOR | 07/23/2012 |
| K122323 | SIEMENS HEALTHCARE DIAGNOSTICS | DIMENSION VISTA ALKALINE PHOSPHATASE (ALPI) FLEX REAGENT CARTRIDGE DIMENSION VISTA ALKALINE PHOSPHATASE CALIBRATOR (ALPI | 08/28/2012 |
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