FDA 510(k) Applications for Medical Device Product Code "GQP"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K981226 | DAKO DIAGNOSTICS LTD. | IMAGEARAINFLUENZA VIRUS GROUP (TYPES 1,2 AND 3) TEST AND IMAGEN PARAINFLUENZA VIRUS TEST TYPES 1,2 AND 3 | 09/28/1998 |