The Siesta Group North America

The Siesta Group North America holds 1 FDA 510(k) medical device clearance, cleared in 2009.

Top product codes for The Siesta Group North America

MNR — Anesthesiology1 device

Recent clearances by The Siesta Group North America

K083620 — SOMNOLYZER 24X7Code MNR·2009-03-06

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