P.T. Healthcare Glovindo is one of 6 FDA 510(k) medical device manufacturers from Indonesia in the dataset, ranked by real submission volume.
P.T. Healthcare Glovindo - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
P.T. Healthcare Glovindo has 7 FDA 510(k) cleared medical devices. Based in Jakarta, ID.
Historical record: 7 cleared submissions from 1993 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by P.T. Healthcare Glovindo Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - P.T. Healthcare Glovindo
7 devices
Cleared
Aug 12, 2002
PRE-POWDERED LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM (180 UG/OR...
General Hospital
84d
Cleared
Sep 21, 2001
PRE-POWDERED NITRILE EXAMINATION GLOVES
General Hospital
240d
Cleared
Jun 22, 2001
POWDER FREE NITRILE EXAMINATION GLOVES
General Hospital
149d
Cleared
Oct 23, 2000
DIGITCARE POWDER FREE COATED EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING...
General Hospital
223d
Cleared
Feb 09, 1998
LATEX (POWDER FREE) LOW PROTEIN
General Hospital
42d
Cleared
Oct 21, 1993
POWDER-FREE PATIENT EXAMINATION GLOVES
General Hospital
216d
Cleared
Aug 16, 1993
POWDERED EXAMINATION GLOVES
General Hospital
172d