RecallHawk

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

Becton Dickinson and Company

Summary

Becton Dickinson and Company received 510(k) clearance for BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton Broth, a JTZ device. Cleared on 2026-09-14.

Details

Source

510(k) Clearance

External ID

K262163

Action Date

2026-09-14

Status

Traditional

Category

device

Product Code

JTZ

Product Description

BD BBL Mueller Hinton II Broth (Cation-Adjusted); BD Difco Mueller Hinton Broth. Product code: JTZ.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 445 device clearances issued this month. Becton Dickinson and Company has received 45 total clearances in our database.

Becton Dickinson and Company has 49 FDA actions in our database, including 4 recalls and 45 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Becton Dickinson and Company have FDA actions?

Becton Dickinson and Company has 49 FDA actions in our database, including 4 recalls and 45 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K262163" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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