Rhytec Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rhytec Incorporated - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Rhytec Incorporated has 5 FDA 510(k) cleared medical devices. Based in North Reading, US.
Historical record: 5 cleared submissions from 2006 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Rhytec Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rhytec Incorporated
5 devices
Cleared
Aug 22, 2008
RHYTEC, INC., PORTRAIT PSR
General & Plastic Surgery
18d
Cleared
Mar 27, 2008
PORTRAIT PSR, MODEL 745915
General & Plastic Surgery
143d
Cleared
Sep 12, 2007
PORTRAIT STAND-OFF
General & Plastic Surgery
16d
Cleared
Jul 26, 2007
PORTRAIT PSR
General & Plastic Surgery
24d
Cleared
Sep 05, 2006
PORTRAIT PSR3
General & Plastic Surgery
152d