Cardio Metrics Cardiotomy Reservoir

FDA 510(k) K841958 · Sterile Design, Inc.

Substantially Equivalent

510(k) numberK841958

Submission

Device name
Cardio Metrics Cardiotomy Reservoir
Applicant
Sterile Design, Inc.
Oldsmar, FL, US
Received
May 14, 1984
Decision date
October 15, 1984
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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K993060Gas FilterJOD · Traditional Olson Medical Sales, Inc.03/28/2000SE
K890504Cardiotomy/Autotransfusion/Pleural Drainage VenousJOD · Traditional Gish Biomedical, Inc.03/10/1989SE
K875095Pall Cardioplegia Plus Filter W/Posidyne MembraneJOD · Traditional Pall Biomedical Products Co.02/29/1988SE
K874405Pall Stat Prime(Tm) Blood Filter for Extra. UseJOD · Traditional Pall Biomedical Products Co.12/30/1987SE
K855067Swank Cardiotomy Suction Line Blood Filter CA100JOD · Traditional Cobe Laboratories, Inc.02/26/1986SE
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

More from Medical, Inc.

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K841959Cardio Metric Custom Perfusion TubingDWE · Traditional 10/19/1984SE
K842351Sterile Design-Custom Sterile IV KitFPA · Traditional 10/15/1984SE
K834239Sdi C-Flex Sterile Light Handle · Traditional 04/25/1984SE
K834237Graduated Guide Wire Bowl 8DQX · Traditional 02/04/1984SE
K813437Pan SetFRG · Traditional 12/31/1981SE
K791738Custom Dressing Change TraysFMC · Traditional 10/02/1979SE

Questions and answers

When was Cardio Metrics Cardiotomy Reservoir cleared by the FDA?

Cardio Metrics Cardiotomy Reservoir (K841958) received a 510(k) decision of Substantially Equivalent on October 15, 1984, 154 days after the submission was received.

What is the product code of K841958?

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.