Dr. Boo Co., Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Dr. Boo Co., Ltd. General Hospital ✕
4 devices
Cleared
Jun 21, 1994
DR. BOO POWDER-FREE LATEX EXAM GLOVES
General Hospital
98d
Cleared
May 04, 1989
PATIENT EXAMINATION GLOVES
General Hospital
55d
Cleared
Mar 22, 1989
PATIENT EXAMINATION GLOVE (LATEX)
General Hospital
13d
Cleared
Mar 21, 1989
PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
14d