FDA 510(k) Applications Submitted by LASEROPTEK CO. LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K152856 | 09/29/2015 | Helios III | LASEROPTEK CO. LTD. |
| K083203 | 10/30/2008 | HELIOS II Q-SWITCHED ND:YAG LASER SYSTEM | LASEROPTEK CO. LTD. |
| K083253 | 11/04/2008 | LOTUS II PULSED ER: YAG LASER SYSTEM | LASEROPTEK CO. LTD. |
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