Globe Ent., Inc. is one of 7619 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Globe Ent., Inc. - FDA 510(k) Cleared Devices
Recent clearances: PROTOS 100ML BURETTE INFUSION SET/ PROTOS 150ML BURETTE INFUSION SET, PROTOS I.V. ADMINISTRATION SET (15 DROPS/ML) I4070S/(60 DROPS/ML)I4670S PRELIMINARY, PROTOS BLOOD TRANSFUSION SET
5
Total
5
Cleared
0
Denied
Globe Ent., Inc. has 5 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 5 cleared submissions from 1989 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Globe Ent., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Globe Ent., Inc.
5 devices
Cleared
Dec 17, 1997
PROTOS 100ML BURETTE INFUSION SET/ PROTOS 150ML BURETTE INFUSION SET
General Hospital
138d
Cleared
Dec 17, 1997
PROTOS I.V. ADMINISTRATION SET (15 DROPS/ML) I4070S/(60 DROPS/ML)I4670S...
General Hospital
138d
Cleared
Dec 16, 1997
PROTOS BLOOD TRANSFUSION SET
General Hospital
137d
Cleared
Sep 11, 1989
PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
154d
Cleared
Mar 14, 1989
SURGICAL GLOVES
General Hospital
130d