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FDA 510(k)

SAPHENOUS VEIN IRRIGATION, PRESSURIZATIO

K-Number: K790938 · 1979-06-13

ApplicantShiley, Inc.
Decision Date1979-06-13
Product CodeDWP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SAPHENOUS VEIN IRRIGATION, PRESSURIZATIO is the device name listed in this FDA 510(k) record. The listed applicant is Shiley, Inc.. It received FDA 510(k) clearance on 1979-06-13 under 510(k) number K790938. The device is classified under product code DWP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAPHENOUS VEIN IRRIGATION, PRESSURIZATIO?

SAPHENOUS VEIN IRRIGATION, PRESSURIZATIO is a medical device that received FDA 510(k) clearance on 1979-06-13. The listed applicant is Shiley, Inc.. The 510(k) number is K790938.

When did SAPHENOUS VEIN IRRIGATION, PRESSURIZATIO receive FDA 510(k) clearance?

SAPHENOUS VEIN IRRIGATION, PRESSURIZATIO received FDA 510(k) clearance on 1979-06-13, under 510(k) number K790938.

Who is the listed applicant for SAPHENOUS VEIN IRRIGATION, PRESSURIZATIO?

The FDA 510(k) record lists Shiley, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAPHENOUS VEIN IRRIGATION, PRESSURIZATIO?

The FDA product code for SAPHENOUS VEIN IRRIGATION, PRESSURIZATIO is DWP.

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Other records listing Shiley, Inc. as applicant

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Related Devices (Code: DWP)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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