FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

COOL LINE CATHETER KIT, MODELS CL-2085B, CL-2295A; ICY CATHETER KIT, MODEL IC-3585A; FORTIUS CATHETER KIT, MOD. FR-5093B

K Number: K051912 · Decision Oct 11, 2005
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
25
Applicant Total
9
Review Days
89

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Basic Information

Device Name
COOL LINE CATHETER KIT, MODELS CL-2085B, CL-2295A; ICY CATHETER KIT, MODEL IC-3585A; FORTIUS CATHETER KIT, MOD. FR-5093B
K Number
K051912
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5900
Medical Specialty
Cardiovascular
Decision
Unknown
Statement or Summary
Summary
Applicant
Alsius Corp.
Date Received
July 14, 2005
Decision Date
October 11, 2005
Product Code
NCX
Advisory Committee
Cardiovascular
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
NCX System, Hypothermia, Intravenous, Cooling

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Other Clearances by Alsius Corp.

K Number Device Name
K081936 SOLEX CATHETER, MODEL SL2593
K072234 THERMOGARD XP THERMAL REGULATION SYSTEM
K070161 QUATTRO CATHETER MODEL IC4593
K063829 THERMOGARD THERMAL REGULATION SYSTEM
K060308 COOLGARD 3000
K052443 ICY CATHETER, MODEL IC-3893A
K030421 ALSIUS COOLGARD 3000 & ALSIUS CATHETER SYSTEM
K014241 COOLGARD 3000, COOLINE, START-UP, MODELS 3000, CL-2085B, CL-2295A, CG-500D