FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GUIDE WIRE FOR EDI CATHETER, 8FR,125CM,5 EACH,GUIDE WIRE FOR EDI CATHETER, 8FR,125CM,5 EACH,GUIDE WIRE FOR EDI CATHETER,

K Number: K101199 · Decision Aug 27, 2010
Classifications
1
FEI Numbers
242
Registration Numbers
243
Same Product Code
648
Applicant Total
14
Review Days
120

Basic Information

Device Name
GUIDE WIRE FOR EDI CATHETER, 8FR,125CM,5 EACH,GUIDE WIRE FOR EDI CATHETER, 8FR,125CM,5 EACH,GUIDE WIRE FOR EDI CATHETER,
K Number
K101199
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MAQUET CRITICAL CARE AB
Date Received
April 29, 2010
Decision Date
August 27, 2010
Product Code
KNT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KNT Tubes, Gastrointestinal (And Accessories)

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K123149 SERVO-I VENTILATOR SYSTEM
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K102182 MAQUET FLOW-I C20, MAQUET FLOW-I C30, MODEL 66 77 200, 66 77 30
K073179 SERVO-I VENTILATOR SYSTEM MODEL 64 87 800 E4073, HELIOX OPTION, MODEL 6675585
K063404 SERVO-I VENTILATOR SYSTEM, MODELS 64, 87 AND 800
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