Professional Instruments 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) | K864830 | TEFLON-COATED HYPODERMIC NEEDLES/REGIONAL BLOCK | BXN | 1987-01-12 | View |
| 510(k) | K864829 | MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT | BXN | 1987-01-12 | View |
| 510(k) | K810206 | DUAL TYPE ELECTRODE | GXY | 1981-03-20 | View |
No matching devices.
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