Jeneric Ind.

FDA 510(k) & PMA Approved Devices — 25 products

Total Devices25

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K862822	REXILLIUM N. B. F.	EJH	1986-09-02	View
510(k)	K862926	SURGICAL VITEX	ELE	1986-08-29	View
510(k)	K854878	H40 BASE METAL ALLOY	EJH	1986-01-30	View
510(k)	K844123	RX CBY	EJH	1985-01-09	View
510(k)	K844122	RX CBG	EJH	1985-01-09	View
510(k)	K840563	RX C & B 20	EJS	1984-05-01	View
510(k)	K840561	RX ELAN	EJS	1984-05-01	View
510(k)	K840562	REX V	EJH	1984-04-13	View
510(k)	K834560	VITEX P.D.A	EJH	1984-02-27	View
510(k)	K833774	NATURELLE II & LITE II-N72-N74-L	EJS	1984-01-24	View
510(k)	K833736	GOLD-PALLADIUM-SILVER BASED CAST/ALLOY	EIS	1983-12-29	View
510(k)	K833143	REXILLIUM III	EJH	1983-12-08	View
510(k)	K833145	ZENITH	EJH	1983-11-28	View
510(k)	K833052	RXG	EJT	1983-11-14	View
510(k)	K833053	Y CERAMIC	EJT	1983-11-14	View
510(k)	K833049	PALLADENT	EJS	1983-10-28	View
510(k)	K833144	REX ALLOY	EJH	1983-10-28	View
510(k)	K833050	RX 90	EJS	1983-10-28	View
510(k)	K823008	NOVAREX	EJH	1982-11-03	View
510(k)	K822947	NEPTUNE	EJH	1982-10-26	View