Mennen Medical , Ltd.
Mennen Medical , Ltd. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2015.
Top product codes for Mennen Medical , Ltd.
Recent clearances by Mennen Medical , Ltd.
- K141441 — MENNTOR X7
- K131789 — CEREBRALOGIK- AEEG
- K123792 — HORIZON XVU (FFR)
- K093766 — VITALOGIK 6000/6500
- K091165 — HORIZON XVU
- K083063 — BIS INTERFACE FOR VITALOGIK PATIENT MONITORS
- K081484 — HORIZON XVU
- K073140 — VITALOGIK MODEL 4000/4500
- K071899 — BIS MODULE FOR ENVOY PATIENT MONITOR
- K071348 — EMS-XL CARDIAC ELECTROPHYSIOLOGY SYSTEM
- K070254 — HORIZON SE
- K052288 — VITALOGIK
- K043564 — HORIZON ANGIO CATHLAB
- K024245 — ENVOY PATIENT MONITOR
- K032997 — MODIFICATION TO: HORIZON 9000WS
- K023798 — MODIFICATION TO ENVOY PATIENT MONITOR
- K022168 — ENVOY
- K020632 — ENGUARD REMOTE PATIENT MONITOR
- K011784 — MODIFICATION TO ENVOY PATIENT MONITOR
- K001120 — ENVOY PATIENT MONITOR
- K000563 — MODIFICATION TO ENVOY PATIENT MONITOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.