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BD MAX Vaginal Panel, BD MAX System, BD Molecular Swab Collection Kit

Geneohm Sciences Canada, Inc. (Bd Life Sciences)

Summary

Geneohm Sciences Canada, Inc. (Bd Life Sciences) received 510(k) clearance for BD MAX Vaginal Panel, BD MAX System, BD Molecular Swab Collection Kit, a PQA device. Cleared on 2021-10-18.

Details

Source

510(k) Clearance

External ID

K201017

Action Date

2021-10-18

Status

Traditional

Category

device

Product Code

PQA

Product Description

BD MAX Vaginal Panel, BD MAX System, BD Molecular Swab Collection Kit. Product code: PQA.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month.

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 Geneohm Sciences Canada, Inc. (Bd Life Sciences) have FDA actions?

This is the only FDA action we have on record for Geneohm Sciences Canada, Inc. (Bd Life Sciences) in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K201017" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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