The following data is part of a premarket notification filed by Becton, Dickinson & Co. with the FDA for Bd Phoenix Automated Microbiology System-cefepime (gn) 0.5-65 Ug/ml.
Device ID | K032675 |
510k Number | K032675 |
Device Name: | BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-CEFEPIME (GN) 0.5-65 UG/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 | 2003-08-29 |
Decision Date | 2004-03-01 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
30382904488032 | K032675 | 000 |
30382904488025 | K032675 | 000 |