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

NOVA Patient Warming System

K Number: K203085 · Decision Nov 12, 2020
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
157
Applicant Total
4
Review Days
30

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Basic Information

Device Name
NOVA Patient Warming System
K Number
K203085
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Encompass Group, LLC
Date Received
October 13, 2020
Decision Date
November 12, 2020
Product Code
DWJ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

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

Product Code Device Name
DWJ System, Thermal Regulating

Similar 510(k) Clearances

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

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Other Clearances by Encompass Group, LLC

K Number Device Name
K982058 ROTECNO FR (FLUID RESISTANT) SURGICAL GOWN
K982059 ROTECNO 2000 SURGICAL GOWN
K760618 PATIENT RESTRAINT