FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

KING LTS REUSABLE OROPHARYNGEAL AIRWAY WITH DRAIN/SUCTION CHANNEL, MODELS KLT 303, KLT 304 AND KLT 305

K Number: K033189 · Decision May 4, 2004
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
56
Applicant Total
18
Review Days
216

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Basic Information

Device Name
KING LTS REUSABLE OROPHARYNGEAL AIRWAY WITH DRAIN/SUCTION CHANNEL, MODELS KLT 303, KLT 304 AND KLT 305
K Number
K033189
Device Class
FDA class 1
Clearance Type
Special
Regulation Number
868.5110
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
King Systems Corp.
Date Received
October 1, 2003
Decision Date
May 4, 2004
Product Code
CAE
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CAE Airway, Oropharyngeal, Anesthesiology

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Other Clearances by King Systems Corp.

K Number Device Name
K033186 KING LT-D DISPOSABLE OROPHARYNGEAL AIRWAY, MODELS KLT 203, KLT 204 AND KLT 205
K021634 KING LT, MODELS # KLT 100, KLT 101, KLT 102, KLT 103, KLT 104, KLT 105
K012485 MS-140 ALL-ROUND ENHANCED PERFORMANCE FILTER; MS-141 ALL-ROUND ENHANCED PERFORMANCE ANGLED; MS-142 ALL-ROUND/HME ENHANCE
K010040 SLEEVED FILTER
K990614 HME-BOOSTER
K983817 BREATHING CIRCUIT BACTERIAL FILTER/HEAT AND MOISTURE EXCHANGER (HME/F)
K973797 BREATHING CIRCUIT BACTERIAL FILTER
K953513 XENON CIRCUIT
K951093 KAB SYSTEM
K950318 FLEX BLUE
Search all 18 clearances from King Systems Corp. →