FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CARESCAPE Central Station V2

K Number: K162012 · Decision Sep 15, 2016
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
77
Applicant Total
168
Review Days
56

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Basic Information

Device Name
CARESCAPE Central Station V2
K Number
K162012
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Healthcare
Date Received
July 21, 2016
Decision Date
September 15, 2016
Product Code
DXJ
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
DXJ Display, Cathode-Ray Tube, Medical

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