Cleared Traditional

K250862 - EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-XP190) (FDA 510(k) Clearance)

Also includes:
EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-P190) EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-XT190) BRONCHOVIDEOSCOPE (OLYMPUS BF-H1100) BRONCHOVIDEOSCOPE (OLYMPUS BF-1TH1100)
Jun 2025
Decision
94d
Days
Class 2
Risk

K250862 is an FDA 510(k) clearance for the EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-XP190). This device is classified as a Bronchoscope (flexible Or Rigid) (Class II - Special Controls, product code EOQ).

Submitted by Olympus Medical Systems Corp. (Tokyo, JP). The FDA issued a Cleared decision on June 23, 2025, 94 days after receiving the submission on March 21, 2025.

This device falls under the Ear, Nose, Throat FDA review panel. Regulated under 21 CFR 874.4680. 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)..

Submission Details

510(k) Number K250862 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 21, 2025
Decision Date June 23, 2025
Days to Decision 94 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).

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