FDA 510(k) Applications for Medical Device Product Code "GHM"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K960947 | SA SCIENTIFIC, INC. | SAS SICKLE CELL TEST | 07/01/1996 |
K013316 | STRECK LABORATORIES, INC. | SICKLE-CHEX | 11/06/2001 |
K023656 | STRECK LABORATORIES, INC. | SICKLE-CHEX SOLUBILITY KIT | 12/30/2002 |