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

GUAVA II

K Number: K122632 · Decision Feb 11, 2014
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
9
Review Days
531

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Basic Information

Device Name
GUAVA II
K Number
K122632
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cardiocomm Solutions, Inc.
Date Received
August 29, 2012
Decision Date
February 11, 2014
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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K111320 GLOBALCARDIO
K033037 MODIFICATION TO GLOBALCARDIO
K022297 GLOBAL ECG MANAGEMENT SYSTEM (GEMS)
K020366 GLOBAL ECG MANAGEMENT SYSTEM (GEMS)
K013354 GLOBALCARDIO