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

Epicardia Anywhere

K Number: K173170 · Decision Jan 10, 2018
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
23
Review Days
103

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Basic Information

Device Name
Epicardia Anywhere
K Number
K173170
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicomp, Inc.
Date Received
September 29, 2017
Decision Date
January 10, 2018
Product Code
DSI
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
DSI Detector And Alarm, Arrhythmia

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Other Clearances by Medicomp, Inc.

K Number Device Name
K161916 TelePatch Cardiac Monitor
K091696 SAVI WIRELESS, MODEL PM500
K090834 EPICARDIA 5000
K043454 CARDIOPAL AI WITH DIOGENES SV (CARDIOPAL SV), MODEL PM410
K981119 CARDIOPAL MODEL NUMBER PM20
K952846 EPICARDIA
K943915 HEAT AND MOISTURE EXCHANGER FILTER (HME)
K900207 EPICARDIA 4000
K883103 EPICARDIA PC/FC
K881770 EPICARDIA LE/FD
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