Intl. Diagnostic, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
Advertisement
Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K841853 | PREG-BETA ONE HOUR TUBE TEST | JHJ | 1984-06-22 | View |
| 510(k) | K840833 | PREG BETA BLUS SLIDE | JHJ | 1984-05-30 | View |
| 510(k) | K834584 | NABI CRP-Q.S. TEST | DCN | 1984-02-27 | View |
| 510(k) | K840005 | NABI RF-Q.S. TEST | DHR | 1984-02-13 | View |
| 510(k) | K802343 | PREGNA B-ANTI HUMAN CHORIONIC GONADOTRO | JHJ | 1980-10-10 | View |
| 510(k) | K780321 | PREGNANCY TEST KIT, OVER-THE-COUNTER | LCX | 1978-04-04 | View |
No matching devices.
Advertisement