Medical Device Manufacturer · US , Milford , CT

Cardiopulmonary Corp. - FDA 510(k) Cleared Devices

9 submissions · 6 cleared · Since 1995

Total

Cleared

Denied

Cardiopulmonary Corp. has 6 FDA 510(k) cleared medical devices. Based in Milford, US.

Historical record: 6 cleared submissions from 1995 to 2013. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Cardiopulmonary Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Cardiopulmonary Corp.

9 devices

1-9 of 9

Cleared Dec 20, 2013

BERNOULLI ENTERPRISE SOFTWARE

K130208 · MHX

Cardiovascular · 326d

Cleared Aug 14, 2009

BERNOULLI MANAGEMENT SYSTEM, OXINET III AND LIFEGARD VUE

K091461 · MOD

Anesthesiology · 88d

Cleared Sep 14, 2006

BERNOULLI MANAGEMENT SYSTEM (MS) SOFTWARE

K061932 · MSX

Cardiovascular · 69d

Cleared Jun 23, 2005

MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWARE

K051283 · MSX

Cardiovascular · 37d

Cleared Feb 21, 2002

MODIFICATION TO BERNOULLI VENTILATOR MANAGEMENT SYSTEM SOFTWARE

K020018 · MSX

Cardiovascular · 49d

Cleared Nov 06, 2001

BERNOULLI VENTILATOR MANAGEMENT SYSTEM

K011861 · MOD

Anesthesiology · 145d

Cleared Feb 24, 1999

MODIFICATION OF VENTURI VENTILATOR

Anesthesiology · 459d

Cardiopulmonary Corp. - FDA 510(k) Cleared Devices

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