RecallHawk

STA R Max 3, STA Compact Max 3

Diagnostica Stago S.A.S

Summary

Diagnostica Stago S.A.S received 510(k) clearance for STA R Max 3, STA Compact Max 3, a JPA device. Cleared on 2023-06-07.

Details

Source

510(k) Clearance

External ID

K212183

Action Date

2023-06-07

Status

Traditional

Category

device

Product Code

JPA

Product Description

STA R Max 3, STA Compact Max 3. Product code: JPA.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 534 device clearances issued this month. Diagnostica Stago S.A.S has received 2 total clearances in our database.

Diagnostica Stago S.A.S has 2 FDA actions in our database, including 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 Diagnostica Stago S.A.S have FDA actions?

Diagnostica Stago S.A.S has 2 FDA actions in our database, including 0 recalls and 2 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K212183" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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