King Systems Corp. is one of 5632 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
King Systems Corp. - FDA 510(k) Cleared Devices
Recent clearances: KING LTS REUSABLE OROPHARYNGEAL AIRWAY WITH DRAIN/SUCTION CHANNEL, MODELS KLT 303, KLT 304 AND KLT 305, KING LT-D DISPOSABLE OROPHARYNGEAL AIRWAY, MODELS KLT 203, KLT 204 AND KLT 205, KING LT, MODELS # KLT 100, KLT 101, KLT 102, KLT 103, KLT 104, KLT 105
18
Total
18
Cleared
0
Denied
King Systems Corp. has 18 FDA 510(k) cleared medical devices. Based in Noblesville, US.
Historical record: 18 cleared submissions from 1988 to 2004. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by King Systems Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - King Systems Corp.
18 devices
Cleared
May 04, 2004
KING LTS REUSABLE OROPHARYNGEAL AIRWAY WITH DRAIN/SUCTION CHANNEL, MODELS KLT...
Anesthesiology
216d
Cleared
Apr 14, 2004
KING LT-D DISPOSABLE OROPHARYNGEAL AIRWAY, MODELS KLT 203, KLT 204 AND KLT 205
Anesthesiology
196d
Cleared
Jan 09, 2003
KING LT, MODELS # KLT 100, KLT 101, KLT 102, KLT 103, KLT 104, KLT 105
Anesthesiology
237d
Cleared
Oct 09, 2001
MS-140 ALL-ROUND ENHANCED PERFORMANCE FILTER
General Hospital
68d
Cleared
Mar 09, 2001
SLEEVED FILTER
General Hospital
63d
Cleared
May 23, 2000
HME-BOOSTER
Anesthesiology
453d
Cleared
Mar 01, 1999
BREATHING CIRCUIT BACTERIAL FILTER/HEAT AND MOISTURE EXCHANGER (HME/F)
General Hospital
123d
Cleared
Mar 12, 1998
BREATHING CIRCUIT BACTERIAL FILTER
General Hospital
157d
Cleared
Nov 03, 1995
XENON CIRCUIT
Radiology
100d
Cleared
Mar 24, 1995
KAB SYSTEM
Anesthesiology
15d
Cleared
Feb 13, 1995
FLEX BLUE
Anesthesiology
18d
Cleared
Aug 19, 1994
K.P.R. (KING PERSONAL RESUSCITATOR)
Anesthesiology
36d