The following data is part of a premarket notification filed by Medic Sharplight Ltd. with the FDA for Beamax.
| Device ID | K063249 |
| 510k Number | K063249 |
| Device Name: | BEAMAX |
| Classification | Powered Laser Surgical Instrument |
| Applicant | MEDIC SHARPLIGHT LTD. 6 SIRENI STREET Haifa, IL 32972 |
| Contact | Dan Laor |
| Correspondent | Dan Laor MEDIC SHARPLIGHT LTD. 6 SIRENI STREET Haifa, IL 32972 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-10-26 |
| Decision Date | 2007-01-17 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BEAMAX 77502848 3605370 Dead/Cancelled |
Beamax BVBA 2008-06-19 |
![]() BEAMAX 74359520 2016641 Dead/Cancelled |
JAPAN APPLIED OPTICS INC. 1993-02-16 |
![]() BEAMAX 74327940 1828847 Dead/Cancelled |
THOMAS INDUSTRIES INC. 1992-11-03 |