Palomar Medical Products, Inc.
FDA 510(k) medical device clearances.
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.