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

ALLON 2001 VERSION 5

K Number: K024128 · Decision Feb 10, 2003
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
157
Applicant Total
6
Review Days
56

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Basic Information

Device Name
ALLON 2001 VERSION 5
K Number
K024128
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.5900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mtre Advanced Technology , Ltd.
Date Received
December 16, 2002
Decision Date
February 10, 2003
Product Code
DWJ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DWJ System, Thermal Regulating

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Other Clearances by Mtre Advanced Technology , Ltd.

K Number Device Name
K102112 CRITICOOL PRO
K083662 CRITICOOL
K003349 ALLON 2001 MODIFIED
K001546 ALLON 2001
K992386 ALLON 2000