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.

510(k) submissions have been managed by Mdi Consultants as regulatory consultant.

Medicomp, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

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

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