Vitaid, Ltd.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K050803 | PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBES | BTR | 2005-06-30 | View |
| 510(k) | K932647 | WIRE REINFORCED ENDOTRACHEAL TUBE | BTR | 1993-11-02 | View |
| 510(k) | K901738 | SELFCATH | KOD | 1990-06-27 | View |
| 510(k) | K894883 | PHYCON ALL SILICONE BALLOON CATHETER | EZL | 1990-04-25 | View |
| 510(k) | K894794 | AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP | KPM | 1989-11-21 | View |
| 510(k) | K894669 | LASER SHIELDING TUBE | BTR | 1989-10-13 | View |
| 510(k) | K894337 | UNIVENT TUBE 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MM | CBI | 1989-09-29 | View |
No matching devices.
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