The following data is part of a premarket notification filed by Becton, Dickinson & Co. with the FDA for Bd Phoenix Automated Microbiology System -ampicillin-sulbactam (gn) 0.5/0.25-32/16ug/ml.
Device ID | K043389 |
510k Number | K043389 |
Device Name: | BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM -AMPICILLIN-SULBACTAM (GN) 0.5/0.25-32/16UG/ML |
Classification | System, Test, Automated, Antimicrobial Susceptibility, Short Incubation |
Applicant | BECTON, DICKINSON & CO. 7 LOVETON CIR. Sparks, MD 21152 -0999 |
Contact | Monica E Giguere |
Correspondent | Monica E Giguere 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 | 2004-12-09 |
Decision Date | 2005-01-21 |
Summary: | summary |