Avatron, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Avatron, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1984 to 1985. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Avatron, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Avatron, Inc.
5 devices
Cleared
Jun 14, 1985
ANESTHESIA BREATHING CIRCUIT
Anesthesiology
80d
Cleared
Feb 14, 1985
AVA-MIST PORTABLE AIR COMPRESSOR
Anesthesiology
55d
Cleared
Aug 17, 1984
AVA-NEB NEBULIZER
Anesthesiology
10d
Cleared
Jul 26, 1984
AVATRON UNIVERSAL ADULT VOL. VENTILATOR
Anesthesiology
10d
Cleared
Jun 26, 1984
AVATRON DISPOSABLE I.P.P.B. CIRUCIT
Anesthesiology
8d