Dr. Boo Co., Ltd.

Dr. Boo Co., Ltd. holds 4 FDA 510(k) medical device clearances, first cleared 1989, most recent 1994.

Top product codes for Dr. Boo Co., Ltd.

LYY — General Hospital4 devices

Recent clearances by Dr. Boo Co., Ltd.

K941240 — DR. BOO POWDER-FREE LATEX EXAM GLOVESCode LYY·1994-06-21
K891313 — PATIENT EXAMINATION GLOVESCode LYY·1989-05-04
K891271 — PATIENT EXAMINATION GLOVE (LATEX)Code LYY·1989-03-22
K891242 — PATIENT EXAMINATION GLOVES (LATEX)Code LYY·1989-03-21

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