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

VIEWMATE ULTRASOUND IMAGING SYSTEM

K Number: K031066 · Decision Oct 17, 2003
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
1117
Applicant Total
12
Review Days
197

Basic Information

Device Name
VIEWMATE ULTRASOUND IMAGING SYSTEM
K Number
K031066
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
EP MEDSYSTEMS
Date Received
April 3, 2003
Decision Date
October 17, 2003
Product Code
IYN
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IYN System, Imaging, Pulsed Doppler, Ultrasonic

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K070706 EP-WORKMATE
K063113 EP-WORKMATE
K041442 EP-4 CLINICAL STIMUTATOR
K040207 EP-4 CLINICAL STIMULATOR
K032225 EP-WORKMATE WITH RPM SYSTEM
K991001 MODIFICATION OF PROCATH ELECTROPHYSIOLOGY CATHETER, EP MEDSYSTEMS ELECTROPHYSIOLOGY CATHETER
K984150 PROCATH ELECTROPHYSIOLOGY CATHETER, EP MEDSYSTEMS ELECTROPHYSIOLOGY CATHETER
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