The following data is part of a premarket notification filed by Toa Medical Electronics Usa, Inc. with the FDA for Sysmex F-800 15 Parameter, Semi-auto Hema Analyzer.
Device ID | K873734 |
510k Number | K873734 |
Device Name: | SYSMEX F-800 15 PARAMETER, SEMI-AUTO HEMA ANALYZER |
Classification | Counter, Differential Cell |
Applicant | TOA MEDICAL ELECTRONICS USA, INC. 4410 CERRITOS AVE. Los Alamitos, CA 90720 |
Contact | Paul N Broden |
Correspondent | Paul N Broden TOA MEDICAL ELECTRONICS USA, INC. 4410 CERRITOS AVE. Los Alamitos, CA 90720 |
Product Code | GKZ |
CFR Regulation Number | 864.5220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-09-15 |
Decision Date | 1987-11-25 |