The following data is part of a premarket notification filed by Bayer Healthcare, Llc with the FDA for Advia 60 Hematology Analyzer.
Device ID | K032524 |
510k Number | K032524 |
Device Name: | ADVIA 60 HEMATOLOGY ANALYZER |
Classification | Counter, Differential Cell |
Applicant | BAYER HEALTHCARE, LLC 511 BENEDICT AVE. Tarrytown, NY 10591 |
Contact | Kenneth T Edds |
Correspondent | Kenneth T Edds BAYER HEALTHCARE, LLC 511 BENEDICT AVE. Tarrytown, NY 10591 |
Product Code | GKZ |
CFR Regulation Number | 864.5220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-08-15 |
Decision Date | 2003-09-08 |
Summary: | summary |