P.T. Irama Dinamika Latex is one of 6 FDA 510(k) medical device manufacturers from Indonesia in the dataset, ranked by real submission volume.
P.T. Irama Dinamika Latex - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
P.T. Irama Dinamika Latex has 11 FDA 510(k) cleared general hospital devices. Based in Medan - Indonesia, ID.
Historical record: 11 cleared submissions from 1991 to 1999.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - P.T. Irama Dinamika Latex
11 devices
Cleared
Mar 19, 1999
NATURAL RUBBER PRE-POWDERED COLORED & FLAVORED PATIENT EXAMINATION GLOVES...
General Hospital
95d
Cleared
Nov 05, 1998
POWDERFREE COLORED AND FLAVORED CHLOROPRENE PATIENT EXAMINATION GLOVES
General Hospital
227d
Cleared
Apr 28, 1998
HYPOALLERGENIC LATEX PATIENT EXAM GLOVES-PREPOWDERED
General Hospital
55d
Cleared
Sep 12, 1997
POWDERFREE COLORED AND FLAVORED NITRILE COPOLYMER PATIENT EXAMINATION...
General Hospital
85d
Cleared
Mar 05, 1997
LATEX EXAM GLOVES
General Hospital
72d
Cleared
Dec 19, 1996
NITRILE COPOLYMER PATIENT EXAMINATION GLOVES
General Hospital
175d
Cleared
Dec 19, 1996
CHLOROPRENE EXAM GLOVES
General Hospital
91d
Cleared
Nov 20, 1996
FLAVORED LATEX PATIENT EXAMINATION
General Hospital
302d
Cleared
Jan 04, 1996
PATIENT EXAMINATION GLOVES
General Hospital
164d
Cleared
Oct 19, 1994
LATEX EXAM GLOVES
General Hospital
191d
Cleared
Nov 07, 1991
PATIENT EXAMINATION GLOVES
General Hospital
86d