Saphenous Vein Irrigation, Pressurizatio

FDA 510(k) K790938 · Shiley, Inc.

Substantially Equivalent

510(k) numberK790938

Submission

Device name
Saphenous Vein Irrigation, Pressurizatio
Applicant
Shiley, Inc.
Mchenry, IL, US
Received
May 18, 1979
Decision date
June 13, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DWP – Dilator, Vessel, Surgical
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4475
Specialty
Cardiovascular

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K910923BCD AdvancedDTR · Traditional 04/09/1991SE
K901548Biomedical Sensors-Shiley BGM 4000 Intra Blood GasCCC · Traditional 01/14/1991SE
K903435Shiley Specialized Tracheostomy TubeJOH · Traditional 10/02/1990SE
K901624Shiley Plexus Integral Reservoir Hollow Fiber Oxy.DTZ · Traditional 07/03/1990SE
K901250Plexus 2(TM) Infant Hollow Fiber OxygenatorDTZ · Traditional 06/11/1990SE
K901249Plexus 3.5(TM) Pediatric Hollow Fiber OxygenatorDTZ · Traditional 06/11/1990SE
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Questions and answers

When was Saphenous Vein Irrigation, Pressurizatio cleared by the FDA?

Saphenous Vein Irrigation, Pressurizatio (K790938) received a 510(k) decision of Substantially Equivalent on June 13, 1979, 26 days after the submission was received.

What is the product code of K790938?

The FDA product code is DWP – Dilator, Vessel, Surgical, a Class II (moderate risk) device regulated under 21 CFR 870.4475.