Perstorp AB C/O Robert Joel Slomoff

Perstorp AB C/O Robert Joel Slomoff holds 2 FDA 510(k) medical device clearances, first cleared 1987, most recent 1991.

Top product codes for Perstorp AB C/O Robert Joel Slomoff

KOZ — General, Plastic Surgery2 devices

Recent clearances by Perstorp AB C/O Robert Joel Slomoff

K905069 — IODOSORB GELCode KOZ·1991-01-31
K870559 — IODOSORB POWDERCode KOZ·1987-03-20

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