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

SMARTDOP XT

K Number: K131623 · Decision Jan 17, 2014
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
71
Applicant Total
18
Review Days
227

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Basic Information

Device Name
SMARTDOP XT
K Number
K131623
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2880
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Koven Technology, Inc.
Date Received
June 4, 2013
Decision Date
January 17, 2014
Product Code
JOP
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
JOP Transducer, Ultrasonic

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Other Clearances by Koven Technology, Inc.

K Number Device Name
K201114 Bidop 7
K153762 Smartdop XT6
K143332 Fast Sphyg by Koven
K080178 VALVULOTOME BY KOVEN
K050601 SMARTDOP 45 VASCULAR DOPPLER
K031931 ECHO SOUNDER EX-101EX 8 MHZ
K031504 ECHO SOUNDER, SINGLE-HANDED, MODEL ES-101EX
K023143 ECHO SOUNDER, ES-102EX
K010452 BI-DIRECTIONAL DOPPLER VOLUME FLOWMETER, MODEL DVM-4300 & 4300T
K982986 TUBING BLOOD FLOW METER MODEL NUMBER HD-800
Search all 18 clearances from Koven Technology, Inc. →