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510(k) K790938

Device
Saphenous Vein Irrigation, Pressurizatio
Applicant
SHILEY, INC.
510(k) number
K790938
Product code
DWP
Decision
Substantially Equivalent (SESE)
Decision date
1979-06-13
Date received
1979-05-18
Regulation
870.4475
Classification name
Dilator, Vessel, Surgical
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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K833676SURGICAL VESSEL DILATORS-CATHERIZA-Cimed Intl., Inc.1984-03-19
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