Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton Broth

K-Number: K262163 · 2026-09-14

Decision Date2026-09-14
Product CodeJTZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton Broth is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson and Company. It received FDA 510(k) clearance on 2026-09-14 under 510(k) number K262163. The device is classified under product code JTZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton Broth?

BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton Broth is a medical device that received FDA 510(k) clearance on 2026-09-14. The listed applicant is Becton Dickinson and Company. The 510(k) number is K262163.

When did BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton Broth receive FDA 510(k) clearance?

BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton Broth received FDA 510(k) clearance on 2026-09-14, under 510(k) number K262163.

Who is the listed applicant for BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton Broth?

The FDA 510(k) record lists Becton Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton Broth?

The FDA product code for BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton Broth is JTZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Becton Dickinson and Company as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 101 devices →

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.

↑