Sumirubber Industries (Kedah) Sdn. Bhd.

Sumirubber Industries (Kedah) Sdn. Bhd. holds 3 FDA 510(k) medical device clearances, first cleared 1989, most recent 1999.

Top product codes for Sumirubber Industries (Kedah) Sdn. Bhd.

LZA — General Hospital2 devices
LYY — General Hospital1 device

Recent clearances by Sumirubber Industries (Kedah) Sdn. Bhd.

K984309 — NBR 4 MILS, NITRILE EXAMINATION GLOVE NON-STERILE POWDEREDCode LZA·1999-02-12
K984311 — NBR4 MILS NITRILE POWDER FREE EXAMINATION GLOVES NON-STERILECode LZA·1999-02-09
K890393 — EXAMINATION GLOVESCode LYY·1989-08-10

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