510(k) K260401
K260401 is an FDA 510(k) premarket notification submitted by Olympus Medical Systems Corporation for the device "EVIS EUS ULTRASOUND BRONCHOFIBERVIDEOSCOPE OLYMPUS BF-UCP190F (BF-UCP190F)". The FDA issued a decision of Substantially Equivalent on August 27, 2026. The device falls under product code PSV (Ultrasound Bronchoscope), a Class II device regulated under 21 CFR 892.1550. Olympus Medical Systems Corporation has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 27, 2026
- Date Received
- February 6, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ultrasound Bronchoscope
- Device Class
- Class II
- Regulation Number
- 892.1550
- Review Panel
- EN
- Submission Type
An ultrasound bronchoscope is indicated for the ultrasonic visualization, diagnosis and therapeutic access to the bronchial tree or the lungs. 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).