The following data is part of a premarket notification filed by Becton Dickinson & Co. with the FDA for Bd Phoenix Automated Microbiology System-linezolid-gram Positive.
Device ID | K040006 |
510k Number | K040006 |
Device Name: | BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-LINEZOLID-GRAM POSITIVE |
Classification | System, Test, Automated, Antimicrobial Susceptibility, Short Incubation |
Applicant | BECTON DICKINSON & CO. 7 LOVETON CIR. Sparks, MD 21152 |
Contact | Michelle B Bandy |
Correspondent | Michelle B Bandy BECTON DICKINSON & CO. 7 LOVETON CIR. Sparks, MD 21152 |
Product Code | LON |
CFR Regulation Number | 866.1645 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-01-02 |
Decision Date | 2004-02-27 |
Summary: | summary |