Medical Device Manufacturer · US , Mchenry , IL

Medicomp, Inc. - FDA 510(k) Cleared Devices

23 submissions · 23 cleared · Since 1983

Total

Cleared

Denied

Medicomp, Inc. has 23 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 23 cleared submissions from 1983 to 2018. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Medicomp, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medicomp, Inc.

23 devices

1-12 of 23

Cleared Jan 10, 2018

Epicardia Anywhere

K173170 · DSI

Cardiovascular · 103d

Cleared Dec 21, 2016

TelePatch Cardiac Monitor

K161916 · DRG

Cardiovascular · 162d

Cleared Oct 26, 2009

SAVI WIRELESS, MODEL PM500

K091696 · DRG

Cardiovascular · 138d

CARDIOPAL AI WITH DIOGENES SV (CARDIOPAL SV), MODEL PM410

K043454 · MLO

Cardiovascular · 99d

Cleared Oct 14, 1998

CARDIOPAL MODEL NUMBER PM20

K981119 · DXH

Cardiovascular · 201d

HEAT AND MOISTURE EXCHANGER FILTER (HME)

Cardiovascular · 196d

MEDICOMP STRAIGHT SWIVEL ADAPTOR

K880434 · BZA

Anesthesiology · 59d

Medicomp, Inc. - FDA 510(k) Cleared Devices

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