Pall Cardioplegia Plus Filter W/Posidyne Membrane

FDA 510(k) K875095 · Pall Biomedical Products Co.

Substantially Equivalent

510(k) numberK875095

Submission

Device name
Pall Cardioplegia Plus Filter W/Posidyne Membrane
Applicant
Pall Biomedical Products Co.
Glen Cove, NY, US
Received
December 10, 1987
Decision date
February 29, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JOD – Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4270
Specialty
Cardiovascular

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K841958Cardio Metrics Cardiotomy ReservoirJOD · Traditional Sterile Design, Inc.10/15/1984SE
K830634Cardiotomy FilterJOD · Traditional Texas Medical Products, Inc.06/30/1983SE
K823260Interface Cardiotomy Blood Filter #51JOD · Traditional Medical, Inc.11/24/1982SE
K823259Interface Cardiotomy Blood Filter #50JOD · Traditional Medical, Inc.11/24/1982SE
K812243Interface Cardiotomy Blood Filter #51JOD · Traditional Medical, Inc.08/25/1981SE
K781383Interface Cardiotomy Blood FilterJOD · Traditional Medical, Inc.09/27/1978SE

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K874405Pall Stat Prime(Tm) Blood Filter for Extra. UseJOD · Traditional 12/30/1987SE
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Questions and answers

When was Pall Cardioplegia Plus Filter W/Posidyne Membrane cleared by the FDA?

Pall Cardioplegia Plus Filter W/Posidyne Membrane (K875095) received a 510(k) decision of Substantially Equivalent on February 29, 1988, 81 days after the submission was received.

What is the product code of K875095?

The FDA product code is JOD – Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4270.