The following data is part of a premarket notification filed by Becton, Dickinson & Co. with the FDA for Bd Phoenix Automated Microbiology System-imipenem 1-16 Ug/ml Gram-negative Id/ast Or Ast Only Phoenix Panels.
Device ID | K032275 |
510k Number | K032275 |
Device Name: | BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-IMIPENEM 1-16 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 | Michelle B Bandy |
Correspondent | Michelle B Bandy 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 | 2003-07-23 |
Decision Date | 2003-09-29 |
Summary: | summary |