Arvik Enterprises/ Mini Lap Technologies

Arvik Enterprises/ Mini Lap Technologies holds 1 FDA 510(k) medical device clearance, cleared in 2011.

Top product codes for Arvik Enterprises/ Mini Lap Technologies

GAA — General, Plastic Surgery1 device

Recent clearances by Arvik Enterprises/ Mini Lap Technologies

K102274 — ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENTCode GAA·2011-06-15

Data sourced from openFDA. This site is unofficial and independent of the FDA.