Raymart Development Co.

Raymart Development Co. holds 1 FDA 510(k) medical device clearance, cleared in 1994.

Top product codes for Raymart Development Co.

HGE — Obstetrics/Gynecology1 device

Recent clearances by Raymart Development Co.

K926425 — AMNIPERF(TM)Code HGE·1994-03-07

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