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

SPECTRUM MONITOR, MODEL 0998-00-1000-XXXXX

K Number: K062098 · Decision Feb 5, 2007
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
411
Applicant Total
132
Review Days
196

Basic Information

Device Name
SPECTRUM MONITOR, MODEL 0998-00-1000-XXXXX
K Number
K062098
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DATASCOPE CORP.
Date Received
July 24, 2006
Decision Date
February 5, 2007
Product Code
MHX
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
MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

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