Palomar Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Palomar Medical Products, Inc. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Palomar Medical Products, Inc. has 21 FDA 510(k) cleared general & plastic surgery devices. Based in Cary, US.
Historical record: 21 cleared submissions from 1998 to 2011.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Palomar Medical Products, Inc.
21 devices
Cleared
Nov 14, 2011
EMERGE FRACTIONAL LASER
General & Plastic Surgery
138d
Cleared
Oct 27, 2009
MODIFICATION TO LUX1540 HANDPIECE AND LUX 1440 HANDPIECE
General & Plastic Surgery
165d
Cleared
Aug 20, 2009
THERMAPULSE
Physical Medicine
28d
Cleared
Jun 01, 2009
LOI SYSTEM
General & Plastic Surgery
95d
Cleared
Feb 27, 2009
ERBIUM FRACTIONAL HANDPIECE
General & Plastic Surgery
60d
Cleared
Feb 13, 2009
PALOMAR ASPIRE LASER PLATFORM
General & Plastic Surgery
109d
Cleared
Jun 20, 2008
PALOMAR LUX 1540 HANDPIECE
General & Plastic Surgery
141d
Cleared
May 29, 2008
PALOMAR ASPIRE LASER PLATFORM
General & Plastic Surgery
9d
Cleared
Apr 16, 2008
PALOMAR ASPIRE LASER PLATFORM
General & Plastic Surgery
47d
Cleared
Mar 26, 2008
MODIFICATION TO PALOMAR LUX1540 HANDPIECE
General & Plastic Surgery
97d
Cleared
Nov 05, 2007
ERBIUM FRACTIONAL HANDPIECE
General & Plastic Surgery
129d
Cleared
May 25, 2007
PALOMAR ERBIUM HANDPIECE
General & Plastic Surgery
30d