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 |