The following data is part of a premarket notification filed by Innovaquartz Llc with the FDA for Proflex Laser Fibers (proflex 200) And Proflex Laser Fibers (proflex 273).
| Device ID | K142638 |
| 510k Number | K142638 |
| Device Name: | ProFlex Laser Fibers (ProFlex 200) And ProFlex Laser Fibers (PRoFlex 273) |
| Classification | Powered Laser Surgical Instrument |
| Applicant | InnovaQuartz LLC 23030 North 15th Ave Phoenix, AZ 85027 -1315 |
| Contact | Stephen Griffin |
| Correspondent | Stephen Griffin InnovaQuartz LLC 23030 North 15th Ave Phoenix, AZ 85027 -1315 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-09-17 |
| Decision Date | 2014-12-19 |
| Summary: | summary |