Company ยท CA
Vitaid, Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 2005. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 30, 2005 | K050803 | PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBES Vitaid, Ltd. | BTR |
| Nov 2, 1993 | K932647 | WIRE REINFORCED ENDOTRACHEAL TUBE Vitaid, Ltd. | BTR |
| Jun 27, 1990 | K901738 | SELFCATH Vitaid, Ltd. | KOD |
| Apr 25, 1990 | K894883 | PHYCON ALL SILICONE BALLOON CATHETER Vitaid, Ltd., CA | EZL |
| Nov 21, 1989 | K894794 | AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMP Vitaid, Ltd., CA | KPM |
| Oct 13, 1989 | K894669 | LASER SHIELDING TUBE Vitaid, Ltd., CA | BTR |
| Sep 29, 1989 | K894337 | UNIVENT TUBE 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MM Vitaid, Ltd., CA | CBI |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||