Cleared Traditional

K180970 - Disposable guides KDNG00

K180970 is an FDA 510(k) clearance for Disposable guides KDNG00, manufactured by Koelis. The device is a Class 2 Radiology device with product code ITX cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K180970 · Koelis · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2018
Decision
88d
Days
Class 2
Risk

K180970 is an FDA 510(k) clearance for the Disposable guides KDNG00. Classified as Transducer, Ultrasonic, Diagnostic (product code ITX), Class II - Special Controls.

Submitted by Koelis (Meylan, FR). The FDA issued a Cleared decision on July 10, 2018 after a review of 88 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1570 - the FDA radiology and imaging software 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 Koelis devices

FDA 510(k) Submission Details - K180970

510(k) Number K180970 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 13, 2018
Decision Date July 10, 2018
Days to Decision 88 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
19d faster than avg
Panel avg: 107d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ITX Device Classification - Class 2, Special Controls

Product Code ITX Transducer, Ultrasonic, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1570
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 Radiology devices follow this clearance model.

Regulatory Peers - ITX Transducer, Ultrasonic, Diagnostic

All 326
Devices cleared under the same product code (ITX) and FDA review panel - the closest regulatory comparables to K180970.
Opticross 35 15 MHz Peripheral Imaging Catheter
K200733 · Boston Scientific Corporation · Apr 2020
Envision ultrasound pad and cover
K190802 · Civco Medical Solutions · May 2019
Cook-Swartz Doppler Flow Probe
K171272 · Cook Incorporated · Jul 2018
Reusable guides ranges (PERINE range, NAIL range, CON-LEAD range and LIN-LEAD range) and STEADY PRO range
K171040 · Koelis · Jul 2017
ASTRA TEE Transesophageal Probe Reprocessor, ASTRA VR Endovaginal/Endorectal Probe Reprocessor
K163313 · CIVCO Medical Instruments Co., Inc. · Jun 2017
GTK Disposable Needle Guides
K170741 · Geotek Medikal Ltd Sti · Jun 2017