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

Fast Sphyg by Koven

K Number: K143332 · Decision Apr 14, 2015
Classifications
1
FEI Numbers
175
Registration Numbers
175
Same Product Code
192
Applicant Total
17
Review Days
145

Basic Information

Device Name
Fast Sphyg by Koven
K Number
K143332
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1120
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KOVEN TECHNOLOGY, INC.
Date Received
November 20, 2014
Decision Date
April 14, 2015
Product Code
DXQ
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
DXQ Blood Pressure Cuff

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K031931 ECHO SOUNDER EX-101EX 8 MHZ
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K023143 ECHO SOUNDER, ES-102EX
K010452 BI-DIRECTIONAL DOPPLER VOLUME FLOWMETER, MODEL DVM-4300 & 4300T
K982986 TUBING BLOOD FLOW METER MODEL NUMBER HD-800
K961817 B SMART MODEL 1
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