Sontek Industries, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Sontek Industries, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1981 to 1983. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Sontek Industries, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sontek Industries, Inc.
7 devices
Cleared
Nov 03, 1983
TUBE-TITLE
Anesthesiology
37d
Cleared
Nov 03, 1983
BODIA TRACH-SAF DOUBLE SWIVEL
Anesthesiology
37d
Cleared
Nov 03, 1983
BODIA BRONCH-SAF DOUBLE SWIVEL
Anesthesiology
37d
Cleared
Nov 03, 1983
BITE-BLOCK
Anesthesiology
37d
Cleared
Dec 29, 1981
BODAI SWIVEL Y
Anesthesiology
35d
Cleared
Nov 05, 1981
BODAI PATIENT COMMUNICATOR
Physical Medicine
41d
Cleared
May 27, 1981
BODAI SUCTION -SAFE 4
Anesthesiology
23d