Globe Ent., Inc.

Globe Ent., Inc. holds 5 FDA 510(k) medical device clearances, first cleared 1989, most recent 1997.

Top product codes for Globe Ent., Inc.

Recent clearances by Globe Ent., Inc.

K972839 — PROTOS 100ML BURETTE INFUSION SET/ PROTOS 150ML BURETTE INFUSION SETCode FPA·1997-12-17
K972854 — PROTOS I.V. ADMINISTRATION SET (15 DROPS/ML) I4070S/(60 DROPS/ML)I4670S PRELIMINARYCode FPA·1997-12-17
K972843 — PROTOS BLOOD TRANSFUSION SETCode BRZ·1997-12-16
K892623 — PATIENT EXAMINATION GLOVES (LATEX)Code LYY·1989-09-11
K884622 — SURGICAL GLOVESCode KGO·1989-03-14

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