FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

B-Capta

K Number: K202154 · Decision Apr 1, 2021
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
46
Applicant Total
7
Review Days
241

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Basic Information

Device Name
B-Capta
K Number
K202154
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Livanova Deutschland, GmbH
Date Received
August 3, 2020
Decision Date
April 1, 2021
Product Code
DRY
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
DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass

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