KARL STORZ Mediastinoscopes and Instruments— 510(k) K260003
Substantially EquivalentKarl Storz SE & CO. KG
FDA 510(k) clearance K260003 for KARL STORZ Mediastinoscopes and Instruments, Substantially Equivalent on 2026-03-02. Applicant: Karl Storz SE & CO. KG. Device class: 2.
Clearance details
- Applicant
- Karl Storz SE & CO. KG
- Product code
- Code EWY
- Device class
- Class 2
- Regulation
- 21 CFR 874.4720
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tuttlingen, DE
Recent devices under product code EWY
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