Aek Rubber Product Sdn. Bhd.

Aek Rubber Product Sdn. Bhd. holds 2 FDA 510(k) medical device clearances, cleared in 1989.

Top product codes for Aek Rubber Product Sdn. Bhd.

LYY — General Hospital2 devices

Recent clearances by Aek Rubber Product Sdn. Bhd.

K892279 — PATIENT EXAMINATION GLOVESCode LYY·1989-12-01
K891258 — PATIENT EXAMINATION GLOVES (LATEX)Code LYY·1989-04-25

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