FDA 510(k) Applications for Medical Device Product Code "JEH"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K960840 | C.E. DIAGNOSIS, INC. | C.E. VASCULAR MACHINE | 03/28/1997 |
K022636 | MORGAN SCIENTIFIC, INC. | BODY BOX 5500 | 01/13/2003 |
K072061 | VIASYS HEALTHCARE GMBH | MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY | 04/22/2008 |
K223818 | Vitalograph Ireland Ltd. | Model 9160 VitaloQUB | 05/25/2023 |