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