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

Unity Network ID

K Number: K142840 · Decision Jan 7, 2015
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
305
Applicant Total
168
Review Days
99

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Basic Information

Device Name
Unity Network ID
K Number
K142840
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Healthcare
Date Received
September 30, 2014
Decision Date
January 7, 2015
Product Code
MWI
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
MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

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