The following data is part of a premarket notification filed by Heraeus Lasersonics, Inc. with the FDA for Heraeus Lasersonics Tactilase Sterile Dispos Fiber.
Device ID | K913918 |
510k Number | K913918 |
Device Name: | HERAEUS LASERSONICS TACTILASE STERILE DISPOS FIBER |
Classification | Powered Laser Surgical Instrument |
Applicant | HERAEUS LASERSONICS, INC. 575 COTTONWOOD DR. Milpitas, CA 95035 |
Contact | Robert Milder |
Correspondent | Robert Milder HERAEUS LASERSONICS, INC. 575 COTTONWOOD DR. Milpitas, CA 95035 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-09-03 |
Decision Date | 1991-09-25 |