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Dr. Boo Co., Ltd.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K941240 DR. BOO POWDER-FREE LATEX EXAM GLOVESLYY1994-06-21 View
510(k) K891313 PATIENT EXAMINATION GLOVESLYY1989-05-04 View
510(k) K891271 PATIENT EXAMINATION GLOVE (LATEX)LYY1989-03-22 View
510(k) K891242 PATIENT EXAMINATION GLOVES (LATEX)LYY1989-03-21 View
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