MMZ
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Table, Cystometric, Electric
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.4890
- Medical specialty
- Gastroenterology, Urology
- Adverse events (MAUDE)
- 1997: 2 · 2005: 4 · 2006: 3
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| LITHOSTAR MODULARIS WITH SHOCKWAVE SYSTEM CPLUS (K033335) | Siemens Medical Solutions USA, Inc. | 2003-11-25 |
| BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005 (K954278) | Beta Medical Products, Inc. | 1995-10-02 |
| SYNERGY II (K942445) | Synectics Medical, Inc. | 1994-11-22 |
| MDT UROLOGY TABLE (K942485) | Mdt Corp., Inc. | 1994-08-26 |
Track MMZ automatically
Every clearance here is in the API, with alerts when new ones post.