Medos Hilite Oxygenator, Model 7000 & 7000 LT

FDA 510(k) K082403 · Gish Biomedical, Inc.

Substantially Equivalent

510(k) numberK082403

Submission

Device name
Medos Hilite Oxygenator, Model 7000 & 7000 LT
Applicant
Gish Biomedical, Inc.
Houston, TX, US
Received
August 21, 2008
Decision date
May 15, 2009
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DTZ – Oxygenator, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4350
Specialty
Cardiovascular
Life-sustaining
Yes

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More from Chalice Medical , Ltd.

510(k)DeviceDecision
K090450Medos Hilite Pediatric Oxygenator, Models 2800, 2400 LTDTZ · Traditional 09/18/2009SE
K090449Medos Hilite Infant Oxygenator, Model 1000, 800 LTDTZ · Traditional 09/18/2009SE
K091062Medos Hilite Infant Reservoir, Model MVC 0730DTN · Traditional 08/04/2009SE
K083131Medos Hilite Reservoir, Model: 4030DTN · Traditional 07/30/2009SE
K082082Gish SVR Soft Venous Reservoirs with Ha CoatingDTN · Traditional 02/04/2009SE
K081947Gish CAPVRF44 Hardshell Venous Reservoir with Ha CoatingDTN · Traditional 02/04/2009SE
K080708Vision Hollow Fiber Oxygenator with Ha CoatingDTZ · Traditional 02/02/2009SE
K081838Gish Vision Blood Cardioplegia with Ha CoatingDTR · Traditional 01/26/2009SE
K081881Gish Tubing and Connectors with Ha CoatingDWF · Traditional 01/23/2009SE
K081054Gish Arterial Filter with Ha CoatingDTM · Traditional 01/15/2009SE

Questions and answers

When was Medos Hilite Oxygenator, Model 7000 & 7000 LT cleared by the FDA?

Medos Hilite Oxygenator, Model 7000 & 7000 LT (K082403) received a 510(k) decision of Substantially Equivalent on May 15, 2009, 267 days after the submission was received.

What is the product code of K082403?

The FDA product code is DTZ – Oxygenator, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4350.