Medical Industries America, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Medical Industries America, Inc. has 19 FDA 510(k) cleared anesthesiology devices. Based in Australia 2038, AU.
Historical record: 19 cleared submissions from 1986 to 2005.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
19 devices
Cleared
May 02, 2005
REMREST HEATED HUMIDIFIER
Anesthesiology
13d
Cleared
May 28, 2004
TRANSNEB COMPRESSOR W/NEBULIZER, MODEL 5000
Anesthesiology
317d
Cleared
May 04, 2001
REMREST
Anesthesiology
241d
Cleared
Apr 20, 2001
OPTIMA
Physical Medicine
14d
Cleared
Jan 10, 1997
3050 SPORT-NEB
Anesthesiology
91d
Cleared
Mar 21, 1995
3000 AEROSOL TWO
Anesthesiology
217d
Cleared
Mar 10, 1995
3002 AEROMAX
Anesthesiology
291d
Cleared
Mar 02, 1995
605 VACU-MAX
General & Plastic Surgery
314d
Cleared
Feb 24, 1995
4003 AEROLITE
Anesthesiology
295d
Cleared
Feb 21, 1995
503 MAXI COMPRESSOR
Anesthesiology
372d
Cleared
Apr 23, 1991
SLEEPAP
Anesthesiology
131d
Cleared
Mar 27, 1991
MINI-MICRON CIRCUIT
Anesthesiology
236d
Cleared
Feb 12, 1991
MAXI ASPIRATOR
Anesthesiology
274d
Cleared
Feb 12, 1991
#504 MINI COMPRESSOR
Anesthesiology
161d
Cleared
Apr 26, 1990
MAXI COMPRESSORS
Anesthesiology
72d
Cleared
Apr 16, 1990
EVOLUTION ULTRASONIC
Anesthesiology
301d
Cleared
Oct 19, 1989
SLEEPAP MASK
Anesthesiology
87d
Cleared
Nov 14, 1986
PUSH CUSH
Physical Medicine
24d
Cleared
Nov 14, 1986
C' AIRECUSH SEAT CUSHION
Physical Medicine
24d