Powercrest (M) Sdn. Bhd.

Powercrest (M) Sdn. Bhd. holds 2 FDA 510(k) medical device clearances, first cleared 1989, most recent 1994.

Top product codes for Powercrest (M) Sdn. Bhd.

LYY — General Hospital2 devices

Recent clearances by Powercrest (M) Sdn. Bhd.

K934546 — POWDER-FREE LATEX EXAMINATION GLOVECode LYY·1994-01-07
K891637 — PATIENT EXAMINATION GLOVES (LATEX)Code LYY·1989-04-14

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