Preco, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K853144 | CARD THREE IM TEST ITEM #2035, CARD ONE IM #2036 | KTN | 1985-10-16 | View |
| 510(k) | K852751 | TOLVIDINE RED UNHEATED SERUM SYPHILLIS CARD TEST | GMQ | 1985-08-20 | View |
| 510(k) | K853054 | RF CARD TEST | DHR | 1985-08-01 | View |
| 510(k) | K850604 | PRECO PREGNANCY RAPID CARD TEST, HEM #2028 | JHJ | 1985-04-08 | View |
No matching devices.
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