Stimwave Technologies Inc., Dba Stimq, LLC

Stimwave Technologies Inc., Dba Stimq, LLC holds 1 FDA 510(k) medical device clearance, cleared in 2017.

Top product codes for Stimwave Technologies Inc., Dba Stimq, LLC

GZF — Neurology1 device

Recent clearances by Stimwave Technologies Inc., Dba Stimq, LLC

K171366 — Receiver Kit, Trial Kit, Spare Lead Kit, Sterile Revision Kit, SWAG Kit, SWAG Accessory Kit, Charger KitCode GZF·2017-08-04

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