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Hancock Laboratories, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K801885	HANCOCK * OBTURATORS	DTI	1980-09-09	View
510(k)	K800703	MODIFIED CATHETER PACKAGE	DQO	1980-04-08	View
510(k)	K800122	HANCOCK AORTIC PUNCH	DWS	1980-02-01	View
510(k)	K790534	MERSILENE SUTURES	KRH	1979-03-26	View
510(k)	K780568	DURAN FLEXIBLE RING		1978-05-26	View

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