Vitaid, Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vitaid, Ltd. Anesthesiology ✕
4 devices
Cleared
Jun 30, 2005
PEDIATRIC CUFFED AND UNCUFFED ET TUBES
Anesthesiology
92d
Cleared
Nov 02, 1993
WIRE REINFORCED ENDOTRACHEAL TUBE
Anesthesiology
153d
Cleared
Oct 13, 1989
LASER SHIELDING TUBE
Anesthesiology
81d
Cleared
Sep 29, 1989
UNIVENT TUBE 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MM
Anesthesiology
77d