FDA 510(k) Applications for Medical Device Product Code "LDR"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K971826 | ALEXANDER MFG. CO. | ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500 | 07/03/1997 |
K971865 | ALEXANDER MFG. CO. | ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3P | 07/03/1997 |
K153760 | DEKA RESEARCH & DEVELOPMENT | Volumetric Infusion Controller | 10/03/2016 |
K963136 | HEALTH WATCH, INC. | PACER MODEL 100 INFUSION CONTROLLER | 10/10/1997 |