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

STERIS Patient Warming System

K Number: K200446 · Decision Jun 13, 2020
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
157
Applicant Total
204
Review Days
110

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Basic Information

Device Name
STERIS Patient Warming System
K Number
K200446
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
870.5900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STERIS Corporation
Date Received
February 24, 2020
Decision Date
June 13, 2020
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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