LITHOSTAR MODULARIS WITH SHOCKWAVE SYSTEM CPLUS— 510(k) K033335
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K033335 for LITHOSTAR MODULARIS WITH SHOCKWAVE SYSTEM CPLUS, Substantially Equivalent on 2003-11-25. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code MMZ
- Device class
- Class 2
- Regulation
- 21 CFR 876.4890
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Mavern, PA, US
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