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..
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code MMZ
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Mavern, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.