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Energy Life Systems Corp.

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

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K951933	UROTEK RE-USABLE FIBEROPTIC CABLE	GEX	1995-05-26	View
510(k)	K945560	UROTEK LASER CATHETER	GEX	1995-01-18	View
510(k)	K945563	CONVERTIBLE CONTACT SIDE-FIRING REFRACTIVE FIBER (C-SRF(TM))	GEX	1994-12-15	View
510(k)	K943409	SIDE-FIRING UROLOGIC REFRACTIVE FIBER	GEX	1994-08-23	View
510(k)	K934389	UROTEK LASER CATHETER	GEX	1994-02-03	View

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