K161810 is an FDA 510(k) clearance for the BD BACTEC Standard/10 Aerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial. This device is classified as a System, Blood Culturing (Class I - General Controls, product code MDB).
Submitted by Becton Dickinson (Sparks, US). The FDA issued a Cleared decision on February 9, 2017, 223 days after receiving the submission on July 1, 2016.
This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.2560.
| 510(k) Number | K161810 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 01, 2016 |
| Decision Date | February 09, 2017 |
| Days to Decision | 223 days |
| Submission Type | Traditional |
| Review Panel | Microbiology (MI) |
| Summary | Summary PDF |
| Product Code | MDB - System, Blood Culturing |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 866.2560 |