Gish Arterial Filter with Ha Coating

FDA 510(k) K081054 · Gish Biomedical, Inc.

Substantially Equivalent

510(k) numberK081054

Submission

Device name
Gish Arterial Filter with Ha Coating
Applicant
Gish Biomedical, Inc.
Houston, TX, US
Received
April 14, 2008
Decision date
January 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
DTM – Filter, Blood, Cardiopulmonary Bypass, Arterial Line
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4260
Specialty
Cardiovascular
Life-sustaining
Yes

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More from Sorin Group Italia S.R.L.

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K082403Medos Hilite Oxygenator, Model 7000 & 7000 LTDTZ · Traditional 05/15/2009SE
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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
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Questions and answers

When was Gish Arterial Filter with Ha Coating cleared by the FDA?

Gish Arterial Filter with Ha Coating (K081054) received a 510(k) decision of Substantially Equivalent on January 15, 2009, 276 days after the submission was received.

What is the product code of K081054?

The FDA product code is DTM – Filter, Blood, Cardiopulmonary Bypass, Arterial Line, a Class II (moderate risk) device regulated under 21 CFR 870.4260.