Accutron, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Accutron, Inc. has 5 FDA 510(k) cleared medical devices. Based in Golden, US.
Historical record: 5 cleared submissions from 1997 to 2005. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Accutron, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Nov 23, 2005
ANALGESIA GAS MACHINE, MODEL DIGITAL ULTRA
Anesthesiology
89d
Cleared
Mar 12, 2004
RFS VACUUM GAUGE SCAVENGING CIRCUIT
Anesthesiology
128d
Cleared
Oct 27, 1999
GUARDIAN LOW PRESSURE ALARM ACCESSORY, MODEL 34076
Anesthesiology
98d
Cleared
Mar 28, 1997
PIP LOW PROFILE SCAVENGING SYSTEM(260 AND 261)/UNIVERSAL LOW PROFILE...
Anesthesiology
87d
Cleared
Mar 28, 1997
UNIVERSAL LOW PROFILE NASAL HOODS(1250,1275,1350,1450,1475,1550)
Anesthesiology
81d