Cleared Traditional

K233432 - 10F Sheath and Dilator Set

K233432 is the FDA 510(k) clearance for 10F Sheath and Dilator Set by Argon Medical Devices, Inc.. It is a Class 2 Cardiovascular device (product code DYB) cleared through the Traditional 510(k) pathway after a 57-day FDA review.

K233432 · Argon Medical Devices, Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 2023
Decision
57d
Days
Class 2
Risk

K233432 is an FDA 510(k) clearance for the 10F Sheath and Dilator Set. Classified as Introducer, Catheter (product code DYB), Class II - Special Controls.

Submitted by Argon Medical Devices, Inc. (Athens, US). The FDA issued a Cleared decision on December 8, 2023 after a review of 57 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. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Argon Medical Devices, Inc. devices

Submission Details

510(k) Number K233432 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 12, 2023
Decision Date December 08, 2023
Days to Decision 57 days
Submission Type Traditional
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
68d faster than avg
Panel avg: 125d · This submission: 57d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 391
Devices cleared under the same product code (DYB) and FDA review panel - the closest regulatory comparables to K233432.
SureFlex HD Steerable Sheath, VersaCross HD Steerable Sheath
K231227 · Baylis Medical Company, Inc. · Dec 2023
FlexCath Cross Transseptal Solution
K233691 · Acutus Medical, Inc. · Dec 2023
Intri24 Introducer Sheath (52-101)
K233646 · Inari Medical, Inc. · Dec 2023
14F iSLEEVE Introducer Set
K233503 · Boston Scientific Corporation · Nov 2023
Talon Transseptal Sheath
K231108 · Inari Medical, Inc. · Sep 2023
Thinline Sheath Introducer
K232260 · Inneuroco, Inc. · Sep 2023