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FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K020881	MODIFICATION TO PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT	FRN	2002-03-27	View
510(k)	K010824	PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT	MEB	2001-06-05	View
510(k)	K990208	PERSONAL INFUSOR WITH DRUG DISPOSAL SEPTAL PORT	MEG	1999-03-25	View
510(k)	K971362	PERSONAL INFUSOR	MEB	1997-12-04	View

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