Vitaid, Ltd.
Vitaid, Ltd. has 0 FDA recalls, 0 inspections, 7 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Jun 30, 2005
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 7 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 25, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K050803 | PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBES | Jun 30, 2005 |
| K932647 | WIRE REINFORCED ENDOTRACHEAL TUBE | Nov 2, 1993 |
| K901738 | SELFCATH | Jun 27, 1990 |
| K894883 | PHYCON ALL SILICONE BALLOON CATHETER | Apr 25, 1990 |
| K894794 | AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP | Nov 21, 1989 |
| K894669 | LASER SHIELDING TUBE | Oct 13, 1989 |
| K894337 | UNIVENT TUBE 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MM | Sep 29, 1989 |