Aequitron Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODEL AMI INFANT CENTRAL APHEA/HEART RATE MONITOR, MODEL LP-1000 VOLUME VENTILATOR, OXYGEN CONCENTRATION INDICATOR
24
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Aequitron Medical, Inc. Anesthesiology ✕
15 devices
Cleared
Apr 18, 1997
MODEL AMI INFANT CENTRAL APHEA/HEART RATE MONITOR
Anesthesiology
333d
Cleared
Jun 20, 1996
MODEL LP-1000 VOLUME VENTILATOR
Anesthesiology
364d
Cleared
Nov 08, 1994
OXYGEN CONCENTRATION INDICATOR
Anesthesiology
48d
Cleared
Sep 10, 1992
MODEL 6213 REMOTE ALARM
Anesthesiology
343d
Cleared
Mar 11, 1992
PORTABLE OXYGEN GENERATOR
Anesthesiology
103d
Cleared
Apr 10, 1991
RESPIRATION/HEART RATE MONITOR MODEL 9500/9550
Anesthesiology
273d
Cleared
Nov 30, 1990
CONTINUOUS VOLUME VENTILATOR MODEL LP10
Anesthesiology
142d
Cleared
Nov 30, 1990
MODEL LP6 VENTILATOR, MODIFICATION
Anesthesiology
10d
Cleared
Jul 13, 1990
MODEL 9200 RESPIRATION/HEART RATE MONITOR
Anesthesiology
94d
Cleared
Jul 13, 1990
MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON
Anesthesiology
17d
Cleared
Jan 30, 1989
MODEL 9550/9500 RESPIRATION/HEART RATE MONITOR
Anesthesiology
84d
Cleared
Jun 10, 1988
MODEL 9216 RESPIRATION/HEART RATE MONITOR
Anesthesiology
78d
Cleared
Oct 09, 1987
MODEL NUMBER 9216 RESPIRATION/HEART RATE MONITOR
Anesthesiology
72d
Cleared
Jun 05, 1987
MODEL NUMBER 8200 RESPIRATION/HEART RATE MONITOR
Anesthesiology
44d
Cleared
Aug 02, 1985
MEDICON MODEL 8200 AMS(APNEA MONITOR SYSTEM)
Anesthesiology
10d