D6ZO Disposable Heat Exchanger

FDA 510(k) K813264 · Electromedics, Inc.

Substantially Equivalent

510(k) numberK813264

Submission

Device name
D6ZO Disposable Heat Exchanger
Applicant
Electromedics, Inc.
Mchenry, IL, US
Received
November 20, 1981
Decision date
July 6, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DTR – Heat-Exchanger, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4240
Specialty
Cardiovascular
Life-sustaining
Yes

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K250150VANGUARD Blood cardioplegia Systems (Vanguard 4:1 Blood cardioplegia set); VANGUARD…DTR · Special Sorin Group Italia S.R.L.05/30/2025SE
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K223879Quantum PureFlow Standard Heat Exchangers (HX11W-S2, HX11W-S1M and HX11W-S2M)DTR · Special Quara S.R.L.04/13/2023SE
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K201984MPS 3 ND Myocardial Protection SystemDTR · Traditional Quest Medical, Inc.11/20/2020SE
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K930154EL2-SERIES Blood Collection ReervoirDTN · Traditional 07/01/1993SE
K926250Electromedics El-Series Cardiotomy ReservoirDTN · Traditional 02/19/1993SE
K925412Electromedics Tissue Trap/ #TT280BYZ · Traditional 02/05/1993SE
K915737Autotransfusion Blood Collection ReservoirDTN · Traditional 09/03/1992SE
K910238Portable Auto Transfusion System 500CAC · Traditional 06/19/1991SE
K910935Modified Pyrogen TestingDTM · Traditional 05/16/1991SE

Questions and answers

When was D6ZO Disposable Heat Exchanger cleared by the FDA?

D6ZO Disposable Heat Exchanger (K813264) received a 510(k) decision of Substantially Equivalent on July 6, 1982, 228 days after the submission was received.

What is the product code of K813264?

The FDA product code is DTR – Heat-Exchanger, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4240.