The following data is part of a premarket notification filed by Beckman Coulter, Inc. with the FDA for Coulter Lh 750 Hematology Analyzer, Model 6605632.
Device ID | K061574 |
510k Number | K061574 |
Device Name: | COULTER LH 750 HEMATOLOGY ANALYZER, MODEL 6605632 |
Classification | Counter, Differential Cell |
Applicant | BECKMAN COULTER, INC. 11800 SW 147TH AVE. M/S 31-B06 Miami, FL 33196 -2500 |
Contact | Nancy Nadler |
Correspondent | Nancy Nadler BECKMAN COULTER, INC. 11800 SW 147TH AVE. M/S 31-B06 Miami, FL 33196 -2500 |
Product Code | GKZ |
CFR Regulation Number | 864.5220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-06-07 |
Decision Date | 2006-07-21 |
Summary: | summary |