Medical Device Manufacturer · US , Milwaukee , WI

Marquette Medical Systems, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1997

Total

Cleared

Denied

Marquette Medical Systems, Inc. has 9 FDA 510(k) cleared medical devices. Based in Milwaukee, US.

Historical record: 9 cleared submissions from 1997 to 1999. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Marquette Medical Systems, Inc.

9 devices

1-9 of 9

Cleared Dec 06, 1999

QUANTITATIVE SENTINEL SYSTEM

K993008 · HGM

Obstetrics & Gynecology · 90d

Cleared Oct 06, 1998

QT DISPERSION AND T WAVE ANALYSIS PROGRAM (QT GUARD ANALYSIS SYSTEM)

K981024 · LOS

Cardiovascular · 201d

Cleared May 07, 1998

MUSE CARDIOVASCULAR INFORMATION SYSTEM

MULTI-LINK CABLE AND LEAD WIRE SYSTEMS

Cardiovascular · 184d

Cleared Feb 06, 1998

ACUTE CARDIAC ISCHEMIA TIME-INSENSITIVE PREDICTIVE INSTRUMENT (ACI-TIPI) OPTION

K974199 · LOS

Cardiovascular · 88d

Cleared Jan 16, 1998

RAC 2A MODULE HOUSING

K973984 · CCK

Anesthesiology · 88d

Cleared May 08, 1997

DASH 1000 PATIENT MONITOR

K970545 · DSI

Cardiovascular · 85d

Marquette Medical Systems, Inc. - FDA 510(k) Cleared Devices

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