The following data is part of a premarket notification filed by Fotona D.d. with the FDA for Fotona Qx Nd:yag/ktp Laser System Family.
| Device ID | K083889 |
| 510k Number | K083889 |
| Device Name: | FOTONA QX ND:YAG/KTP LASER SYSTEM FAMILY |
| Classification | Powered Laser Surgical Instrument |
| Applicant | FOTONA D.D. STEGNE 7, Ljubljana, SI 1210 |
| Contact | Stojan Trost |
| Correspondent | Stojan Trost 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 | 2008-12-29 |
| Decision Date | 2009-04-23 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 03830054230064 | K083889 | 000 |