Medical Device Manufacturer · US , Noblesville , IN

King Systems Corp. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1988

Total

Cleared

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

1-12 of 18

Cleared May 04, 2004

KING LTS REUSABLE OROPHARYNGEAL AIRWAY WITH DRAIN/SUCTION CHANNEL, MODELS KLT...

K033189 · CAE

Anesthesiology · 216d

Cleared Apr 14, 2004

KING LT-D DISPOSABLE OROPHARYNGEAL AIRWAY, MODELS KLT 203, KLT 204 AND KLT 205

K033186 · CAE

Anesthesiology · 196d

Cleared Jan 09, 2003

KING LT, MODELS # KLT 100, KLT 101, KLT 102, KLT 103, KLT 104, KLT 105

K021634 · CAE

Anesthesiology · 237d

Cleared Oct 09, 2001

MS-140 ALL-ROUND ENHANCED PERFORMANCE FILTER

K012485 · CAH

General Hospital · 68d

Cleared Mar 09, 2001

SLEEVED FILTER

K010040 · CAH

General Hospital · 63d

Cleared May 23, 2000

HME-BOOSTER

K990614 · BTT

Anesthesiology · 453d

Cleared Mar 01, 1999

BREATHING CIRCUIT BACTERIAL FILTER/HEAT AND MOISTURE EXCHANGER (HME/F)

K983817 · CAH

General Hospital · 123d

Cleared Mar 12, 1998

BREATHING CIRCUIT BACTERIAL FILTER

K973797 · CAH

General Hospital · 157d

K.P.R. (KING PERSONAL RESUSCITATOR)

K943402 · CBP

Anesthesiology · 36d

King Systems Corp. - FDA 510(k) Cleared Devices

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