Energy Life Systems Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Energy Life Systems Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Energy Life Systems Corp. has 5 FDA 510(k) cleared medical devices. Based in Costa Mesa, US.
Historical record: 5 cleared submissions from 1994 to 1995. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Energy Life Systems Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Energy Life Systems Corp.
5 devices
Cleared
May 26, 1995
UROTEK RE-USABLE FIBEROPTIC CABLE
General & Plastic Surgery
31d
Cleared
Jan 18, 1995
UROTEK LASER CATHETER
General & Plastic Surgery
79d
Cleared
Dec 15, 1994
CONVERTIBLE CONTACT SIDE-FIRING REFRACTIVE FIBER (C-SRF(TM))
General & Plastic Surgery
38d
Cleared
Aug 23, 1994
SIDE-FIRING UROLOGIC REFRACTIVE FIBER
General & Plastic Surgery
40d
Cleared
Feb 03, 1994
UROTEK LASER CATHETER
General & Plastic Surgery
147d