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Medcor, Inc.

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K792609	LITHICRON 0520 P-SYNCHRONEOUS PULSE GEN.	DXY	1980-11-19	View
510(k)	K802224	QUINTREX 0516 PROG. PULSE GENERATOR SYS		1980-09-12	View
510(k)	K802223	QUINTREX 0515 PROGRAMMABLE PULSE GEN.		1980-09-12	View
510(k)	K791678	LITHICRON II 0403 IMPLANTABLE PACEMAKER	DXY	1979-09-07	View
510(k)	K791095	LITHICRON MODEL 0401, PACEMAKER	DXY	1979-08-10	View
510(k)	K780430	LITHICRON F PROGRAMMABLE PULSE GEN	DXY	1978-12-22	View
510(k)	K771538	LITHICRON MODEL 3-70C-B PULSE GENERATOR	DXY	1977-08-22	View
510(k)	K770507	PULSE GENERATOR, LITKICRON MODEL 3-70H	DXY	1977-04-07	View

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