Asclepion Laser Technologies GmbH
FDA 510(k) medical device clearances.
Top product codes for Asclepion Laser Technologies GmbH
Recent clearances by Asclepion Laser Technologies GmbH
- K261094 — YellowStar
- K253100 — MultiPulse TFL
- K240831 — MultiCut Solo
- K241600 — Dermablate
- K240816 — MeDioStar
- K231876 — MultiPulse HoPLUS
- K213597 — MultiCut Solo
- K213889 — PicoStar
- K210634 — MCL 31 Dermablate System
- K192483 — MeDioStar
- K161257 — MultiPulse HoPLUS
- K152153 — MicroSpot Handpiece
- K150140 — MCL 31 Dermablate
- K143519 — The MeDioStar NeXT Family
- K133891 — MULTIPULSE TM+1470
- K131987 — MULTIPULSE HOPLUS
- K131757 — TATTOOSTAR EFFECT COMBO
- K133297 — QUADROSTARPROGREEN, QUADROSTARPROYELLOW
- K113489 — ORION
- K112669 — TATTOOSTAR EFFECT Y
- K111851 — MEDIOSTAR NEXT
- K081541 — DERMABLATE EFFECT
- K071451 — TATTOOSTAR Y
- K060787 — TATTOOSTAR FAMILY
- K060455 — MULTISTAR
- K060457 — QUADROSTAR 532
- K060459 — QUADROSTAR 980
- K050900 — MEDIOSTAR XT
- K042968 — MCL 30 DERMABLATE ER:YAG LASER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.