Tri/Bor Medical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Tri/Bor Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Westtown, US.
Historical record: 5 cleared submissions from 1991 to 1991. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Tri/Bor Medical, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Apr 01, 1991
MICRO-VENT NEBULIZER SYSTEM
Anesthesiology
165d
Cleared
Apr 01, 1991
AERO-GEN NUBULIZER SYSTEM
Anesthesiology
165d
Cleared
Jan 02, 1991
OXYGEN/AIR TUBING
Anesthesiology
76d
Cleared
Jan 02, 1991
AERO-GEN NEBULIZER
Anesthesiology
76d
Cleared
Jan 02, 1991
DISPOSABLE FACE MASK
Anesthesiology
76d