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FDA 510(k)

BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial

K-Number: K173873 · 2018-03-16

Decision Date2018-03-16
Product CodeMDB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BD BACTEC Peds Plus/F Culture Vials Soybean-Casein Digest Broth with Resins in a Plastic Vial is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2018-03-16 under approval number K173873. The device is classified under product code MDB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.