The following data is part of a premarket notification filed by Becton Dickinson & Co. with the FDA for Bd Phoenix Automated Microbiology System - Ceftazidime 0.5-64 Ug/ml-gram-negative Id/ast Or Ast Only Phoenix Panels.
Device ID | K033560 |
510k Number | K033560 |
Device Name: | BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM - CEFTAZIDIME 0.5-64 UG/ML-GRAM-NEGATIVE ID/AST OR AST ONLY PHOENIX PANELS |
Classification | System, Test, Automated, Antimicrobial Susceptibility, Short Incubation |
Applicant | BECTON DICKINSON & CO. 7 LOVETON CIR. Sparks, MD 21152 -0999 |
Contact | Kathryn Babka Powers |
Correspondent | Kathryn Babka Powers BECTON DICKINSON & CO. 7 LOVETON CIR. Sparks, MD 21152 -0999 |
Product Code | LON |
CFR Regulation Number | 866.1645 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-11-12 |
Decision Date | 2004-01-14 |
Summary: | summary |