Laseroptek Co., Ltd.
FDA 510(k) medical device clearances.
Top product codes for Laseroptek Co., Ltd.
Recent clearances by Laseroptek Co., Ltd.
- K243780 — HELIOS 785 Pico (1754V2)
- K230373 — HELIOS 785 Pico
- K223588 — PALLAS Premium
- K212663 — HELIOS IV 785
- K212573 — PicoLO Premium
- K203491 — PicoLO Nd: YAG Picosecond Laser System
- K191501 — PALLAS 308/311 Solid-State UV Laser System
- K183392 — PicoLO Nd:YAG Picosecond Laser System
- K182045 — Lotus III Multi-Pulsed Er: Yag Laser System
- K172639 — PALLAS 308/311 Solid-State UV Laser System
- K152856 — Helios III
- K083253 — LOTUS II PULSED ER: YAG LASER SYSTEM
- K083203 — HELIOS II Q-SWITCHED ND:YAG LASER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.