Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Microcatheter

K-Number: K232647 · 2023-09-29

Decision Date2023-09-29
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Microcatheter is a medical device manufactured by Surmodics,Inc.. It received FDA 510(k) clearance on 2023-09-29 under approval number K232647. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Microcatheter?

Microcatheter is a medical device that received FDA 510(k) clearance on 2023-09-29. It is manufactured by Surmodics,Inc.. The 510(k) number is K232647.

When was Microcatheter approved by the FDA?

Microcatheter received FDA 510(k) clearance on 2023-09-29, under approval number K232647.

What company makes Microcatheter?

Microcatheter is manufactured by Surmodics,Inc..

What is the FDA product code for Microcatheter?

The FDA product code for Microcatheter is DQY.

Other Devices by Surmodics,Inc.

View all 12 devices →

Related Devices (Code: DQY)

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.