The following data is part of a premarket notification filed by Fotona D.d. with the FDA for Paradigm-fotona Yaplase Nd:yap Laser System And Accessories.
Device ID | K002884 |
510k Number | K002884 |
Device Name: | PARADIGM-FOTONA YAPLASE ND:YAP LASER SYSTEM AND ACCESSORIES |
Classification | Powered Laser Surgical Instrument |
Applicant | FOTONA D.D. STEGNE 7, Ljubljana, SI 1210 |
Contact | Mojca Valjavec |
Correspondent | Mojca Valjavec FOTONA D.D. STEGNE 7, Ljubljana, SI 1210 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-09-15 |
Decision Date | 2000-12-04 |