BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial
K-Number: K173873 · 2018-03-16
Device Summary
Frequently Asked Questions
What is the BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial?
BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial is a medical device that received FDA 510(k) clearance on 2018-03-16. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K173873.
When was BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial approved by the FDA?
BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial received FDA 510(k) clearance on 2018-03-16, under approval number K173873.
What company makes BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial?
BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial is manufactured by Becton, Dickinson and Company.
What is the FDA product code for BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial?
The FDA product code for BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial is MDB.
Other Devices by Becton, Dickinson and Company
Related Devices (Code: MDB)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.