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

CHILLBUSTER

K Number: K022903 · Decision Nov 27, 2002
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
157
Applicant Total
24
Review Days
85

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Basic Information

Device Name
CHILLBUSTER
K Number
K022903
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Microtek Medical, Inc.
Date Received
September 3, 2002
Decision Date
November 27, 2002
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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