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FDA 510(k)

Socrates 38 Catheter

K-Number: K242301 · 2024-12-04

ApplicantScientia Vascular, Inc.
Decision Date2024-12-04
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Socrates 38 Catheter is a medical device manufactured by Scientia Vascular, Inc.. It received FDA 510(k) clearance on 2024-12-04 under approval number K242301. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Socrates 38 Catheter?

Socrates 38 Catheter is a medical device that received FDA 510(k) clearance on 2024-12-04. It is manufactured by Scientia Vascular, Inc.. The 510(k) number is K242301.

When was Socrates 38 Catheter approved by the FDA?

Socrates 38 Catheter received FDA 510(k) clearance on 2024-12-04, under approval number K242301.

What company makes Socrates 38 Catheter?

Socrates 38 Catheter is manufactured by Scientia Vascular, Inc..

What is the FDA product code for Socrates 38 Catheter?

The FDA product code for Socrates 38 Catheter is QJP.

Other Devices by Scientia Vascular, Inc.

K223913Socrates Aspiration System K223560Plato 17 Microcatheter K231954Aristotle 18 Guidewire; Aristotle 24 Guidewire K222437Aristotle Colossus Guidewire K243938Aristotle 14 Guidewire; Aristotle 18 Guidewire; Aristotle 24 Guidewire; Zoom Wire 14 Guidewire; Aristotle Colossus Guidewire K253579Aristotle 14 Guidewire; Aristotle 18 Guidewire; Aristotle 24 Guidewire; Zoom Wire 14 Guidewire

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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.

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