FDA 510(k) Applications for Medical Device Product Code "JHJ"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K972606 | IMMUNOSTICS, INC. | PREGNACOL PREGNANCY TEST | 08/29/1997 |
K921968 | TECH-CO, INC. | IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST | 06/28/1996 |