Medical Device Manufacturer · US , Naples , FL

Aculux - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2000

Recent clearances: ACULUX, MODEL AX3001, AX3002

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aculux General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Jun 23, 2000

ACULUX, MODEL AX3001, AX3002

General & Plastic Surgery · 67d