FDA 510(k) Applications for Medical Device Product Code "GQH"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K982311 | INTRACEL CORP. | BARTELS CINAKIT CMV ANTIGENEMIA | 12/14/1998 |
K964875 | VIRAL ANTIGENS, INC. | CMV ANTIGEN CONTROL SLIDES | 03/18/1997 |