Medical Device Manufacturer · US , Walker , MI

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

82 submissions · 81 cleared · Since 1980

Total

Cleared

Denied

Marquette Electronics, Inc. has 81 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.

Historical record: 81 cleared submissions from 1980 to 1997.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

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

82 devices

1-12 of 82

Cleared Nov 13, 1997

IMPACT (INFORMING MOBILE PERSONNEL AND CARE TRACKING) PAGER SYSTEM

K971868 · MSX

Cardiovascular · 177d

Cleared Oct 22, 1997

WIRELESS LAN (LOCAL AREA NETWORK) - WIRELESS ETHERNET

K971683 · MSX

Cardiovascular · 168d

Cleared Sep 25, 1997

SIGNAL-AVERAGED HIGH RESOLUTION P WAVE ANALYSIS

K972199 · DPS

Cardiovascular · 106d

Cleared Mar 06, 1997

CARDIOSERV P

K962547 · DRO

Cardiovascular · 251d

Cleared Feb 28, 1997

RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEM

K963120 · DRO

Cardiovascular · 200d

Cleared Feb 24, 1997

ALARM DISPLAY UNIT/PAGER-LAN SYSTEM (ADU)

K962827 · DSI

Cardiovascular · 220d

Cleared Feb 21, 1997

EAGLE 4000 PATIENT MONITOR

Cardiovascular · 144d

Cleared Oct 02, 1996

EAGLE 3000/3100 PATIENT MONITOR

K960272 · MLD

Cardiovascular · 258d

Cleared Oct 02, 1996

EAGLE PATIENT MONITOR

K960418 · DSI

Cardiovascular · 247d

Cleared Aug 09, 1996

EAGLE PATIENT MONITOR MODEL 3000/3100

K961139 · DSI

Cardiovascular · 141d

Cleared Aug 08, 1996

BODYTRODE

K961288 · DRX

Cardiovascular · 126d

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

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