Globe Ent., Inc.

FDA Regulatory Profile

Globe Ent., Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 17, 1997.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K972839PROTOS 100ML BURETTE INFUSION SET/ PROTOS 150ML BURETTE INFUSION SETDecember 17, 1997
K972854PROTOS I.V. ADMINISTRATION SET (15 DROPS/ML) I4070S/(60 DROPS/ML)I4670S PRELIMINARYDecember 17, 1997
K972843PROTOS BLOOD TRANSFUSION SETDecember 16, 1997
K892623PATIENT EXAMINATION GLOVES (LATEX)September 11, 1989
K884622SURGICAL GLOVESMarch 14, 1989