RecallHawk

Auto transfusion (ATS) Chest Drains: Ocean Water Seal Chest Drain, Oasis Dry Suction Water Seal Chest Drain, Express Dry

Atrium Medical Corporation

Summary

Atrium Medical Corporation received 510(k) clearance for Auto transfusion (ATS) Chest Drains: Ocean Water Seal Chest Drain, Oasis Dry Suction Water Seal Chest Drain, Express Dry Seal Chest Drain, a CAC device. Cleared on 2021-09-03.

Details

Source

510(k) Clearance

External ID

K201305

Action Date

2021-09-03

Status

Traditional

Category

device

Product Code

CAC

Product Description

Auto transfusion (ATS) Chest Drains: Ocean Water Seal Chest Drain, Oasis Dry Suction Water Seal Chest Drain, Express Dry Seal Chest Drain. Product code: CAC.

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. Atrium Medical Corporation has received 2 total clearances in our database.

Atrium Medical Corporation has 88 FDA actions in our database, including 86 recalls and 2 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 Atrium Medical Corporation have FDA actions?

Atrium Medical Corporation has 88 FDA actions in our database, including 86 recalls and 2 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K201305" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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