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. It is manufactured by Ra Medical Systems,Inc. The 510(k) number is K220544.
When was DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0) approved by the FDA?
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 approval number K220544.
What company makes 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 manufactured by Ra Medical Systems,Inc.
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.
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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.