Richmann Laboratories

Richmann Laboratories holds 1 FDA 510(k) medical device clearance, cleared in 1989.

Top product codes for Richmann Laboratories

FMF — General Hospital1 device

Recent clearances by Richmann Laboratories

K882975 — RE-VENT ARTERIAL BLOOD SAMPLER AND/OR BIOSAMPLERCode FMF·1989-01-25

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