DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0)
K-Number: K220544 · 2022-06-29
Device Summary
Frequently Asked Questions
What is the DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0)?
DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0) is a medical device that received FDA 510(k) clearance on 2022-06-29. The listed applicant is Ra Medical Systems,Inc. The 510(k) number is K220544.
When did DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0) receive FDA 510(k) clearance?
DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0) received FDA 510(k) clearance on 2022-06-29, under 510(k) number K220544.
Who is the listed applicant for DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0)?
The FDA 510(k) record lists Ra Medical Systems,Inc as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0)?
The FDA product code for DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0) is PDU.
Other records listing Ra Medical Systems,Inc as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: PDU)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.