The Rupp & Bowman Co.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K880973 | MICROLYTE 7 | JFP | 1988-09-07 | View |
| 510(k) | K882081 | SPECIFIC CHEMISTRY ANALYZER | JJE | 1988-07-01 | View |
| 510(k) | K880242 | KONE CALCIUM TEST | CJY | 1988-03-15 | View |
No matching devices.
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