Pharos Life Corporation is one of 622 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Pharos Life Corporation - FDA 510(k) Cleared Devices
Recent clearances: TANDA MAX OTC SYSTEM, TANDA MAX, TANDA RESTORE, MODEL PTSCS
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
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