Siemens Medical Solutions USA, Inc. · Class II · Cleared Nov 25, 2003
| K-number | K033335 |
| Device name | LITHOSTAR MODULARIS WITH SHOCKWAVE SYSTEM CPLUS |
| Applicant | Siemens Medical Solutions USA, Inc. |
| Product code | MMZ |
| Device class | Class II |
| Decision date | Nov 25, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 876.4890 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov