Wako Intl., 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) | K790768 | WAKO CHOLESTEROL TEST | CHH | 1979-05-23 | View |
| 510(k) | K781899 | UREA NITROGEN TEST | CDL | 1978-12-20 | View |
| 510(k) | K781629 | SERI-SEP SERUM/PLASMA ISLOLATOR | JKA | 1978-10-27 | View |
| 510(k) | K781342 | GLUCOSE TEST | CGA | 1978-08-31 | View |
No matching devices.
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