Scimed Encore Advantage Kit and the Essentials Kit

FDA 510(k) K951802 · Scimed Life Systems, Inc.

Substantially Equivalent

510(k) numberK951802

Submission

Device name
Scimed Encore Advantage Kit and the Essentials Kit
Applicant
Scimed Life Systems, Inc.
Maple Grove, MN, US
Received
April 19, 1995
Decision date
July 21, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DXT – Injector And Syringe, Angiographic
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1650
Specialty
Cardiovascular

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K251788Extension tubeDXT · Traditional Zhuhai DR Medical Instruments Co., Ltd.03/05/2026SE
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Questions and answers

When was Scimed Encore Advantage Kit and the Essentials Kit cleared by the FDA?

Scimed Encore Advantage Kit and the Essentials Kit (K951802) received a 510(k) decision of Substantially Equivalent on July 21, 1995, 93 days after the submission was received.

What is the product code of K951802?

The FDA product code is DXT – Injector And Syringe, Angiographic, a Class II (moderate risk) device regulated under 21 CFR 870.1650.