Vysis
Vysis holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2004.
Top product codes for Vysis
Recent clearances by Vysis
- DEN040010 — VYSIS AUTOVYSION SYSTEM
- K033982 — MODIFICATION TO VYSIS UROVYSION BLADDER CANCER RECURRENCE TEST
- K013785 — UROVYSION BLADDER CANCER RECURRENCE KIT
- K011031 — VYSIS UROVYSION BLADDER CANCER RECURRENCE KIT
- K010288 — ANEUVYSION MULITICOLOR DNA PROBE KIT
- K972200 — ANEUVYSION
- K954214 — CEP X SPECTRUMORANGE\Y SPECTRUMGREEN DNA PROBE KIT
- K962873 — CEP 12 SPECTRUMORANGE DIRECT LABELED CHROMOSOME ENUMERATION DNA PROBE
- K953591 — CEP 8 SPECTRUMORANGE DNA PROBE KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.