Product code MMZ— Gastroenterology, Urology

FDA has cleared 4 devices under product code MMZ between 1994 and 2003, filed by 4 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 20031 clearance
• 19951 clearance
• 19942 clearances

• Synectics Medical, Inc.1 clearance
• Siemens Medical Solutions USA, Inc.1 clearance
• Mdt Corp., Inc.1 clearance
• Beta Medical Products, Inc.1 clearance

• K033335 — LITHOSTAR MODULARIS WITH SHOCKWAVE SYSTEM CPLUSSiemens Medical Solutions USA, Inc.·2003-11-25
• K954278 — BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005Beta Medical Products, Inc.·1995-10-02
• K942445 — SYNERGY IISynectics Medical, Inc.·1994-11-22
• K942485 — MDT UROLOGY TABLEMdt Corp., Inc.·1994-08-26