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Vitaid, Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K050803PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBESJune 30, 2005
K932647WIRE REINFORCED ENDOTRACHEAL TUBENovember 2, 1993
K901738SELFCATHJune 27, 1990
K894883PHYCON ALL SILICONE BALLOON CATHETERApril 25, 1990
K894794AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMPNovember 21, 1989
K894669LASER SHIELDING TUBEOctober 13, 1989
K894337UNIVENT TUBE 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MMSeptember 29, 1989