Pharos Life Corporation is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Pharos Life Corporation - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Pharos Life Corporation has 5 FDA 510(k) cleared medical devices. Based in Cambridge, CA.
Historical record: 5 cleared submissions from 2007 to 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Pharos Life Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pharos Life Corporation
5 devices
Cleared
Aug 03, 2011
TANDA MAX OTC SYSTEM
General & Plastic Surgery
140d
Cleared
Jan 03, 2011
TANDA MAX
General & Plastic Surgery
42d
Cleared
Oct 15, 2009
TANDA RESTORE, MODEL PTSCS
Physical Medicine
286d
Cleared
Nov 14, 2008
TANDA SKINCARE SYSTEM, MODEL: PTSCS
General & Plastic Surgery
256d
Cleared
Aug 21, 2007
TANDA SKINCARE SYSTEM, PLC-001, TANDA BLUE, 414-001, TANDA RED, 660-001
General & Plastic Surgery
214d