RecallHawk

DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101)

Ra Medical Systems,Inc

Summary

Ra Medical Systems,Inc received 510(k) clearance for DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101), a PDU device. Cleared on 2021-07-27.

Details

Source

510(k) Clearance

External ID

K210664

Action Date

2021-07-27

Status

Traditional

Category

device

Product Code

PDU

Product Description

DABRA Laser System (DABRA Laser model RA-308 and DABRA Catheter model 101). Product code: PDU.

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. Ra Medical Systems,Inc has received 2 total clearances in our database.

Ra Medical Systems,Inc 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 Ra Medical Systems,Inc have FDA actions?

Ra Medical Systems,Inc 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 "K210664" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for device

Related Actions