Acutronic Medical Systems AG - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Acutronic Medical Systems AG has 12 FDA 510(k) cleared anesthesiology devices. Based in Jona-Rapper Swril, CH.
Historical record: 12 cleared submissions from 1986 to 2002.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
12 devices
Cleared
Dec 20, 2002
MONSOON CRITICAL CARE JET VENTILATOR AND ACCESSORIES
Anesthesiology
493d
Cleared
Aug 01, 2002
MISTRAL CRITICAL CARE JET VENTILATOR AND ACCESSORIES
Anesthesiology
352d
Cleared
May 03, 1995
AMS 3000M
Anesthesiology
503d
Cleared
Apr 29, 1991
AMS 3000 PORTABLE JET VENTILATOR
Anesthesiology
437d
Cleared
Apr 29, 1991
VS-200S JET VENTILATOR
Anesthesiology
437d
Cleared
Jun 08, 1989
EXTERNAL JET SYNCHRONIZER, MODEL AMS-1010
Anesthesiology
268d
Cleared
Sep 28, 1987
UNIVERSAL JET VENTILATOR MODEL AMS-1000
Anesthesiology
409d
Cleared
Jan 12, 1987
HEATED JET HUMIDIFIER MODEL AMS-1020
Anesthesiology
150d
Cleared
Nov 03, 1986
TRANS- CIRCOTHYROTOMY DEVICE (ACC. RAVUSSIN)
Anesthesiology
130d
Cleared
Oct 22, 1986
DOUBLE LUMEN E T ADAPTOR
Anesthesiology
118d
Cleared
Aug 06, 1986
UNI-JET CONNECTOR
Anesthesiology
41d
Cleared
Jul 10, 1986
SUCTION T CONNECTOR
Anesthesiology
14d