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Technical Resources, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K810572	BLADE, HANDLE, SCALPEL FORCEPS, SURGERY	GES	1981-03-20	View
510(k)	K792473	THERAPETTE, MODEL NO MH-100	GZJ	1979-12-20	View
510(k)	K790805	DRUG ABUSE DIPSTICKS	DIT	1979-06-06	View

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