The following data is part of a premarket notification filed by Toa Medical Electronics Usa, Inc. with the FDA for Sysmex Auto. Blood Cell Counter, Cc-120.
Device ID | K780909 |
510k Number | K780909 |
Device Name: | SYSMEX AUTO. BLOOD CELL COUNTER, CC-120 |
Classification | Counter, Cell, Automated (particle Counter) |
Applicant | TOA MEDICAL ELECTRONICS USA, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | GKL |
CFR Regulation Number | 864.5200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-06-01 |
Decision Date | 1978-06-28 |