FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

CARDIOVIT AT-102 G2

K Number: K183425 · Decision Mar 2, 2020
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
16
Review Days
447

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Basic Information

Device Name
CARDIOVIT AT-102 G2
K Number
K183425
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Schiller AG
Date Received
December 11, 2018
Decision Date
March 2, 2020
Product Code
DPS
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
DPS Electrocardiograph

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K031557 CARDIOVIT AT-102
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