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

THERMOGARD XP THERMAL REGULATION SYSTEM

K Number: K072234 · Decision Aug 23, 2007
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
25
Applicant Total
9
Review Days
13

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Basic Information

Device Name
THERMOGARD XP THERMAL REGULATION SYSTEM
K Number
K072234
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.5900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alsius Corp.
Date Received
August 10, 2007
Decision Date
August 23, 2007
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

Similar 510(k) Clearances

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

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Other Clearances by Alsius Corp.

K Number Device Name
K081936 SOLEX CATHETER, MODEL SL2593
K070161 QUATTRO CATHETER MODEL IC4593
K063829 THERMOGARD THERMAL REGULATION SYSTEM
K060308 COOLGARD 3000
K052443 ICY CATHETER, MODEL IC-3893A
K051912 COOL LINE CATHETER KIT, MODELS CL-2085B, CL-2295A; ICY CATHETER KIT, MODEL IC-3585A; FORTIUS CATHETER KIT, MOD. FR-5093B
K030421 ALSIUS COOLGARD 3000 & ALSIUS CATHETER SYSTEM
K014241 COOLGARD 3000, COOLINE, START-UP, MODELS 3000, CL-2085B, CL-2295A, CG-500D