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FDA 510(k)

DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0)

K-Number: K220544 · 2022-06-29

Decision Date2022-06-29
Product CodePDU
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DABRA Excimer Laser System (DABRA Laser model RA-308 and DABRA Catheter model 2.0) is a medical device manufactured by Ra Medical Systems,Inc. It received FDA 510(k) clearance on 2022-06-29 under approval number K220544. The device is classified under product code PDU. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.