The following data is part of a premarket notification filed by Becton, Dickinson And Company with the FDA for Bd Phoenix Automated Microbiology System-ertapenem 0.0625-8 Mcg/ml.
Device ID | K151320 |
510k Number | K151320 |
Device Name: | BD Phoenix Automated Microbiology System-Ertapenem 0.0625-8 Mcg/ml |
Classification | System, Test, Automated, Antimicrobial Susceptibility, Short Incubation |
Applicant | BECTON, DICKINSON AND COMPANY 7 LOVETON CIRCLE MC 694 Sparks, MD 21152 |
Contact | Monica E. Giguere |
Correspondent | Monica E. Giguere BECTON, DICKINSON AND COMPANY 7 LOVETON CIRCLE MC 694 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 | 2015-05-18 |
Decision Date | 2016-01-15 |
Summary: | summary |