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

KING SYSTEMS HME

K Number: K934441 · Decision Dec 2, 1993
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
72
Applicant Total
18
Review Days
83

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Basic Information

Device Name
KING SYSTEMS HME
K Number
K934441
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
King Systems Corp.
Date Received
September 10, 1993
Decision Date
December 2, 1993
Product Code
BYD
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
BYD Condenser, Heat And Moisture (Artificial Nose)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BYD), ordered by most recent decision date.

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Other Clearances by King Systems Corp.

K Number Device Name
K033189 KING LTS REUSABLE OROPHARYNGEAL AIRWAY WITH DRAIN/SUCTION CHANNEL, MODELS KLT 303, KLT 304 AND KLT 305
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
Search all 18 clearances from King Systems Corp. →