The following data is part of a premarket notification filed by Laser Peripherals Llc. with the FDA for Laser Peripherals Holmium Bare Fibers.
Device ID | K972272 |
510k Number | K972272 |
Device Name: | LASER PERIPHERALS HOLMIUM BARE FIBERS |
Classification | Powered Laser Surgical Instrument |
Applicant | LASER PERIPHERALS LLC. 5484 FELTL RD. Minnetonka, MN 55343 |
Contact | Nancy L Arnold |
Correspondent | Nancy L Arnold LASER PERIPHERALS LLC. 5484 FELTL RD. Minnetonka, MN 55343 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-06-18 |
Decision Date | 1997-07-29 |