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

Quantum Smart Occluder LH (left-hand), Quantum Smart Occluder LH (right-hand)

K Number: K190282 · Decision May 24, 2019
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
51
Applicant Total
15
Review Days
102

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Basic Information

Device Name
Quantum Smart Occluder LH (left-hand), Quantum Smart Occluder LH (right-hand)
K Number
K190282
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4220
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spectrum Medical , Ltd.
Date Received
February 11, 2019
Decision Date
May 24, 2019
Product Code
DTQ
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
DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass

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