Cleared Traditional

Ion Endoluminal System (IF1000)

K252045 · Intuitive Surgical, Inc. · Ear, Nose, Throat

Sep 2025

Decision

85d

Days

Class 2

Risk

About This 510(k) Submission

K252045 is an FDA 510(k) clearance for the Ion Endoluminal System (IF1000), a Bronchoscope (flexible Or Rigid) (Class II — Special Controls, product code EOQ), submitted by Intuitive Surgical, Inc. (Suunyvale, US). The FDA issued a Cleared decision on September 23, 2025, 85 days after receiving the submission on June 30, 2025. This device falls under the Ear, Nose, Throat review panel. Regulated under 21 CFR 874.4680.

Submission Details

510(k) Number	K252045 FDA.gov
FDA Decision	Cleared SESE
Date Received	June 30, 2025
Decision Date	September 23, 2025
Days to Decision	85 days
Submission Type	Traditional
Review Panel	Ear, Nose, Throat (EN)
Summary	Summary PDF

Device Classification

Product Code	EOQ — Bronchoscope (flexible Or Rigid)
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 874.4680
Definition	A Bronchoscope (flexible Or Rigid) And Accessories Is A Tubular Endoscopic Device With Any Of A Group Of Accessory Devices Which Attach To The Bronchoscope And Is Intended To Examine Or Treat The Larynx And Tracheobronchial Tree. If The Device Is Reprocessed, Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission. If The Device Is Reusable, Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission (82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).