Sontek Industries, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K833361TUBE-TITLENovember 3, 1983
K833372BODIA TRACH-SAF DOUBLE SWIVELNovember 3, 1983
K833373BODIA BRONCH-SAF DOUBLE SWIVELNovember 3, 1983
K833374BITE-BLOCKNovember 3, 1983
K813324BODAI SWIVEL YDecember 29, 1981
K812720BODAI PATIENT COMMUNICATORNovember 5, 1981
K811241BODAI SUCTION -SAFE 4May 27, 1981