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

BP-200 PLUS

K Number: K063814 · Decision Mar 7, 2007
Classifications
1
FEI Numbers
420
Registration Numbers
420
Same Product Code
1186
Applicant Total
15
Review Days
75

Basic Information

Device Name
BP-200 PLUS
K Number
K063814
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SCHILLER AG
Date Received
December 22, 2006
Decision Date
March 7, 2007
Product Code
DXN
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
DXN System, Measurement, Blood-Pressure, Non-Invasive

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