The following data is part of a premarket notification filed by Kowa Optimed, Inc. with the FDA for Laser Flare Meter.
Device ID | K913852 |
510k Number | K913852 |
Device Name: | LASER FLARE METER |
Classification | Biomicroscope, Slit-lamp, Ac-powered |
Applicant | KOWA OPTIMED, INC. 20001 SOUTH VERMONT AVE. Torrance, CA 90502 |
Contact | Hiroshi Okada |
Correspondent | Hiroshi Okada KOWA OPTIMED, INC. 20001 SOUTH VERMONT AVE. Torrance, CA 90502 |
Product Code | HJO |
CFR Regulation Number | 886.1850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-08-27 |
Decision Date | 1992-02-07 |