FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium Pressure

K Number: K192838 · Decision Apr 13, 2020
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
36
Applicant Total
15
Review Days
193

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Basic Information

Device Name
Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium Pressure
K Number
K192838
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4380
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spectrum Medical , Ltd.
Date Received
October 3, 2019
Decision Date
April 13, 2020
Product Code
DWA
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
DWA Control, Pump Speed, Cardiopulmonary Bypass

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