The following data is part of a premarket notification filed by Mentor O & O, Inc. with the FDA for Mentor Horizon Low Vision Magnifier.
Device ID | K915340 |
510k Number | K915340 |
Device Name: | MENTOR HORIZON LOW VISION MAGNIFIER |
Classification | System, Reading, Television, Closed-circuit |
Applicant | MENTOR O & O, INC. 3000 LONGWATER DR. Norwell, MA 02061 -1672 |
Contact | Richard L Follett |
Correspondent | Richard L Follett MENTOR O & O, INC. 3000 LONGWATER DR. Norwell, MA 02061 -1672 |
Product Code | HJG |
CFR Regulation Number | 886.5820 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-10-24 |
Decision Date | 1992-03-30 |