Fortress Introducer Sheath SYstem

FDA 510(k) K153197 · Contract Medical International, GmbH

Substantially Equivalent

510(k) numberK153197

Submission

Device name
Fortress Introducer Sheath SYstem
Applicant
Contract Medical International, GmbH
Dresden, DE
Received
November 4, 2015
Decision date
January 11, 2016
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DYB – Introducer, Catheter
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1340
Specialty
Cardiovascular

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K254248Introducer Sheath SetDYB · Traditional Cardiocycle Medical(Suzhou) Co., Ltd.04/23/2026SE
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More from Protaryx Medical, Inc.

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K250439Catapult Guide Sheath; 4F; 15cm (US-34015-F-ST-H); Catapult Guide Sheath; 4F; 45cm…DYB · Special 03/16/2025SE
K240957Catapult Guide SheathDYB · Special 08/14/2024SE
K221914Catapult Guide SheathDYB · Special 07/29/2022SE
K203179Fortress Introducer Sheath SystemDYB · Special 11/20/2020SE
K181463DuraSheath Introducer Sheath SystemDYB · Traditional 12/13/2018SE
K142357DuraSheath Introducer Sheath SystemDYB · Traditional 06/25/2015SE

Questions and answers

When was Fortress Introducer Sheath SYstem cleared by the FDA?

Fortress Introducer Sheath SYstem (K153197) received a 510(k) decision of Substantially Equivalent on January 11, 2016, 68 days after the submission was received.

What is the product code of K153197?

The FDA product code is DYB – Introducer, Catheter, a Class II (moderate risk) device regulated under 21 CFR 870.1340.