510(k) K260003
K260003 is an FDA 510(k) premarket notification submitted by Karl Storz SE & CO. KG for the device "KARL STORZ Mediastinoscopes and Instruments". The FDA issued a decision of Substantially Equivalent on March 2, 2026. The device falls under product code EWY (Mediastinoscope, Surgical), a Class II device regulated under 21 CFR 874.4720. Karl Storz SE & CO. KG has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 2, 2026
- Date Received
- January 2, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mediastinoscope, Surgical
- Device Class
- Class II
- Regulation Number
- 874.4720
- Review Panel
- EN
- Submission Type
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).