Genie Rubber Products Co.

Genie Rubber Products Co. holds 1 FDA 510(k) medical device clearance, cleared in 1989.

Top product codes for Genie Rubber Products Co.

LYY — General Hospital1 device

Recent clearances by Genie Rubber Products Co.

K891267 — PATIENT EXAMINATION GLOVES (LATEX)Code LYY·1989-04-24

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