The following data is part of a premarket notification filed by Optimed, Inc. with the FDA for Optifield I And Ii Automated Perimeters.
Device ID | K884867 |
510k Number | K884867 |
Device Name: | OPTIFIELD I AND II AUTOMATED PERIMETERS |
Classification | Perimeter, Automatic, Ac-powered |
Applicant | OPTIMED, INC. 100 HEGENBERGER RD. SUITE 210 Oakland, CA 94621 |
Contact | Douglas Donaldson |
Correspondent | Douglas Donaldson OPTIMED, INC. 100 HEGENBERGER RD. SUITE 210 Oakland, CA 94621 |
Product Code | HPT |
CFR Regulation Number | 886.1605 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-11-21 |
Decision Date | 1989-03-09 |