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FDA 510(k) Applications Submitted by PT. IRAMA DINAMIKA LATEX
FDA 510(k) Number
Submission Date
Device Name
Applicant
K965155
12/23/1996
LATEX EXAM GLOVES
PT. IRAMA DINAMIKA LATEX
K960315
01/23/1996
FLAVORED LATEX PATIENT EXAMINATION
PT. IRAMA DINAMIKA LATEX
K980848
03/04/1998
HYPOALLERGENIC LATEX PATIENT EXAM GLOVES-PREPOWDERED
PT. IRAMA DINAMIKA LATEX
K981064
03/23/1998
POWDERFREE COLORED AND FLAVORED CHLOROPRENE PATIENT EXAMINATION GLOVES
PT. IRAMA DINAMIKA LATEX
K972306
06/19/1997
POWDERFREE COLORED AND FLAVORED NITRILE COPOLYMER PATIENT EXAMINATION GLOVES-MEDICAL DEVICE
PT. IRAMA DINAMIKA LATEX
K962518
06/27/1996
NITRILE COPOLYMER PATIENT EXAMINATION GLOVES
PT. IRAMA DINAMIKA LATEX
K953462
07/24/1995
PATIENT EXAMINATION GLOVES
PT. IRAMA DINAMIKA LATEX
K984449
12/14/1998
NATURAL RUBBER PRE-POWDERED COLORED & FLAVORED PATIENT EXAMINATION GLOVES WITH PROTEIN LABELLING CLAIM
PT. IRAMA DINAMIKA LATEX
K963771
09/19/1996
CHLOROPRENE EXAM GLOVES
PT. IRAMA DINAMIKA LATEX
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