J.F. Jelenko & Co., Inc.

FDA 510(k) & PMA Approved Devices — 55 products

Total Devices55

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K012303	JEL-20	EJS	2001-08-22	View
510(k)	K002993	HERACERAM	EIH	2000-11-16	View
510(k)	K002645	JEL BIOS PURE	EJT	2000-10-19	View
510(k)	K002222	RD-2104	EJT	2000-08-31	View
510(k)	K001360	SIGNUM	EBF	2000-06-20	View
510(k)	K001260	ALLROUND 55 LF	EJT	2000-05-17	View
510(k)	K001196	JEL BIOS 90 (CODE NAME RD-2401)	EJT	2000-05-11	View
510(k)	K000532	JEL 15	EJS	2000-04-06	View
510(k)	K993136	JEL BIOS 10 (CODE NAME RD-1801)	EJT	1999-10-21	View
510(k)	K993152	JEL BIOS 18 (CODE NAME RD- 1214)	EJT	1999-10-21	View
510(k)	K991564	JELTEMP	EBG	1999-06-23	View
510(k)	K990056	JELDENT MULTICRYL	EBI	1999-03-25	View
510(k)	K984587	ALLROUND-E (CODE NAME RD 1710)	EJS	1999-03-17	View
510(k)	K984140	MAINBOND A	EJT	1999-01-13	View
510(k)	K981244	BW-1 (CODE NAME RD-0807)	EJT	1998-08-13	View
510(k)	K981257	JELFINE-52 (CODE NAME RD-0901)	EJS	1998-08-13	View
510(k)	K981247	SILCAST (CODE NAME RD-0118)	EJS	1998-07-01	View
510(k)	K973881	PROSPECTOR PLUS (CODE NAME : RD-0508)	EJT	1997-11-24	View
510(k)	K971575	BENCHMARK-IV	EJT	1997-06-04	View
510(k)	K971292	JEL-71 PDF	EJT	1997-05-20	View