Palomar Medical Products, Inc.
Palomar Medical Products, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2011.
Top product codes for Palomar Medical Products, Inc.
Recent clearances by Palomar Medical Products, Inc.
- K111840 — EMERGE FRACTIONAL LASER
- K091446 — MODIFICATION TO LUX1540 HANDPIECE AND LUX 1440 HANDPIECE
- K092222 — THERMAPULSE
- K090525 — LOI SYSTEM
- K083900 — ERBIUM FRACTIONAL HANDPIECE
- K083165 — PALOMAR ASPIRE LASER PLATFORM
- K080244 — PALOMAR LUX 1540 HANDPIECE
- K081416 — PALOMAR ASPIRE LASER PLATFORM
- K080567 — PALOMAR ASPIRE LASER PLATFORM
- K073583 — MODIFICATION TO PALOMAR LUX1540 HANDPIECE
- K071768 — ERBIUM FRACTIONAL HANDPIECE
- K071152 — PALOMAR ERBIUM HANDPIECE
- K061652 — PALOMAR LUX1540 HANDPIECE
- K041086 — PALOMAR STARLUX PULSED LIGHT SYSTEM
- K033549 — STARLUX PULSED LIGHT SYSTEM
- K024179 — PALOMAR LIGHTCUBE
- K013028 — PALOMAR SLP 1000
- K982980 — LIGHTSHEER LONG PULSE RUBY LASER
- K980517 — EPILASER NORMAL MODE RUBY LASER
- K980420 — LIGHTSHEER
- K980160 — EPILASER I UPGRADE KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.