Venomidicard Infant/ Pediatric Venous Cardiotomy Reservoir

FDA 510(k) K941215 · Sorin Biomedical, Inc.

Substantially Equivalent

510(k) numberK941215

Submission

Device name
Venomidicard Infant/ Pediatric Venous Cardiotomy Reservoir
Applicant
Sorin Biomedical, Inc.
Irvine, CA, US
Received
March 10, 1994
Decision date
May 10, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DTN – Reservoir, Blood, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4400
Specialty
Cardiovascular

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More from Medtronic, Inc.

510(k)DeviceDecision
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K963758Code 150 Blood Component Collection Set and with Direct Draw LineCAC · Traditional 02/20/1998SE
K964908VRF40 Venous Reservoir with Integral Cardiotomy FilterDTN · Traditional 09/03/1997SE
K964907Venomidicard Pediatric Venous Reservoir with Integralcardiotomy Filter/Midicard…DTN · Traditional 08/21/1997SE
K961869Dideco Newborn/Infant Arterial Filters: D735 Micro 20 and D736 Micro 40DTM · Traditional 08/12/1996SE
K952270Dideco Adult Arterial Filters D732 Micro 20 W/20, D734 Micro 40 W/40 Micron ScreenDTM · Traditional 08/21/1995SE
K945198Dideco Pediatric Arterial FiltersDTM · Traditional 06/27/1995SE
K945065Dideco Flexible Reservoir -- Product Designation 5063DTN · Traditional 05/19/1995SE
K942582Sorin Blood Cardioplegia ConsoleDTQ · Traditional 01/27/1995SE

Questions and answers

When was Venomidicard Infant/ Pediatric Venous Cardiotomy Reservoir cleared by the FDA?

Venomidicard Infant/ Pediatric Venous Cardiotomy Reservoir (K941215) received a 510(k) decision of Substantially Equivalent on May 10, 1995, 426 days after the submission was received.

What is the product code of K941215?

The FDA product code is DTN – Reservoir, Blood, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4400.