FDA 510(k) Applications for Medical Device Product Code "MCE"
(Respiratory Syncytial Virus - Elisa)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K061008 | QUIDEL CORP. | QUICKVUE RSV (20 TEST KIT), MODEL 20193; (2 TEST KIT), MODEL 20199 | 09/08/2006 |
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