Palomar Medical Technologies, Inc.
Palomar Medical Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2013.
Top product codes for Palomar Medical Technologies, Inc.
Recent clearances by Palomar Medical Technologies, Inc.
- K130250 — QYAG LASER SYSTEM
- K120622 — PALOMAR VECTUS LASER
- K110907 — PALOMAR ICON (TM) AESTHETIC SYSTEM
- K103664 — PRIMUS AESTHETIC PLATFORM
- K101506 — LUX1540, LUX1440 & LUX2940 LASER HANDPIECES
- K100270 — ARTISAN AESTHETIC SYSTEM
- K090195 — PALOMAR LUX1540 HANDPIECE
- K070298 — MODIFICATION TO PALOMAR LUXIR HANDPIECE
- K063571 — PALOMAR LUX2940 HANDPIECE
- K060839 — ABC HAIR REMOVAL SYSTEM
- K061436 — PALOMAR Q-YAG 5 ND:YAG LASER SYSTEM
- K060301 — PALOMAR LUX1540 HANDPIECE
- K060069 — PALOMAR LUXIR FRACTIONAL HANDPIECE
- K050370 — PALOMAR LUXIR HANDPIECE
- K041879 — PALOMAR LUX1064 HANDPIECE
- K040081 — PALOMAR LUXV HANDPIECE
- K023967 — PALOMAR Q-YAG ND:YAG LASER SYSTEM
- K020453 — PALOMAR ESTELUX PULSED LIGHT SYSTEM AND PALOMAR COOLROLLER
- K011747 — PALOMAR LC 100 DIODE LASER
- K010580 — PALOMAR SLP 1000
- K003886 — PALOMAR SPALIGHT PULSED LIGHT SYSTEM
- K003460 — PALOMAR CLEAR LIGHT ND: YAG LASER SYSTEM
- K002649 — ARAMIS DERMATOLOGICAL LASER
- K994225 — PALOMAR SLP 2000
Data sourced from openFDA. This site is unofficial and independent of the FDA.