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 |