Medical Device Manufacturer · US , Sudbury , MA

North East Monitoring, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1995

Total

Cleared

Denied

North East Monitoring, Inc. has 10 FDA 510(k) cleared cardiovascular devices. Based in Sudbury, US.

Historical record: 10 cleared submissions from 1995 to 2014.

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 - North East Monitoring, Inc.

10 devices

1-10 of 10

Anesthesiology · 156d

Cleared May 25, 2007

AUTO DETECT FOR TELAHEART DR200/E-A

K070014 · MWJ

Cardiovascular · 142d

Cleared Aug 25, 2006

TELAHEART DIGITAL RECORDER

K061293 · MWJ

Cardiovascular · 108d

Cleared Aug 31, 2004

SD360 DIGITAL RECORDER/SD360 HOLTER DIGITAL RECORDER

General Hospital · 161d

Cleared Jul 31, 1996

NORTHEAST MONITORING DR180

K960925 · DSH

Cardiovascular · 147d

Cleared Apr 19, 1995

HOLTER FOR WINDOWS

K930564 · DQK

Cardiovascular · 805d

North East Monitoring, Inc. - FDA 510(k) Cleared Devices

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