Cleared Special

K250439 - Catapult Guide Sheath (FDA 510(k) Clearance)

Also includes:
4F 15cm (US-34015-F-ST-H) Catapult Guide Sheath 4F 45cm (US-34045-F-ST-H) Catapult Guide Sheath 4F 60cm (US-34060-F-ST-H) Catapult Guide Sheath 4F 90cm (US-34090-F-ST-H) Catapult Guide Sheath 4F 130cm (US-34130-F-ST-H) Catapult Guide Sheath 5F 15cm (US-35015-F-ST-H) Catapult Guide Sheath 5F 45cm (US-35045-F-ST-H) Catapult Guide Sheath 5F 45cm Hockey Stick (US-35045-F-HS-H) Catapult Guide Sheath 5F 45cm Multipurpose (US-35045-F-MP-H) Ca

Class II Cardiovascular device cleared through the Special 510(k) pathway - typically does not require clinical trials.

K250439 · Contract Medical International, GmbH · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2025
Decision
30d
Days
Class 2
Risk

K250439 is an FDA 510(k) clearance for the Catapult Guide Sheath. Classified as Introducer, Catheter (product code DYB), Class II - Special Controls.

Submitted by Contract Medical International, GmbH (Dresden, DE). The FDA issued a Cleared decision on March 16, 2025 after a review of 30 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1340 - the FDA cardiovascular device oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Contract Medical International, GmbH devices

Submission Details

510(k) Number K250439 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 14, 2025
Decision Date March 16, 2025
Days to Decision 30 days
Submission Type Special
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
95d faster than avg
Panel avg: 125d · This submission: 30d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code DYB Introducer, Catheter
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1340
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - DYB Introducer, Catheter

All 700
Devices cleared under the same product code (DYB) and FDA review panel - the closest regulatory comparables to K250439.
Echo Large Bore Introducer Sheath
K260606 · Echo Medical, LLC · Apr 2026
Introducer Sheath Set
K254248 · Cardiocycle Medical(Suzhou) Co., Ltd. · Apr 2026
Edwards eSheath+ introducer set
K254279 · Edwards Lifesciences · Apr 2026
Aventus Introducer Sheath
K260091 · Inquis Medical · Apr 2026
Protaryx Transseptal Puncture Device (PTX2-001)
K260839 · Protaryx Medical, Inc. · Apr 2026
AuST Steerable Sheath
K260942 · CenterPoint Systems, LLC · Apr 2026