The following data is part of a premarket notification filed by Excel Tech. Ltd. with the FDA for Excel Model Xlt-one Nd:yag Laser System.
Device ID | K914849 |
510k Number | K914849 |
Device Name: | EXCEL MODEL XLT-ONE ND:YAG LASER SYSTEM |
Classification | Powered Laser Surgical Instrument |
Applicant | EXCEL TECH. LTD. 101-2 COLIN DR. Holbrook, NY 11741 |
Contact | Dr.rama Rao |
Correspondent | Dr.rama Rao EXCEL TECH. LTD. 101-2 COLIN DR. Holbrook, NY 11741 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-10-28 |
Decision Date | 1992-02-25 |