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FDA 510(k)

Socrates 38 Catheter

K-Number: K242301 · 2024-12-04

Decision Date2024-12-04
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Socrates 38 Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Scientia Vascular, Inc.. It received FDA 510(k) clearance on 2024-12-04 under 510(k) 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. The listed applicant is Scientia Vascular, Inc.. The 510(k) number is K242301.

When did Socrates 38 Catheter receive FDA 510(k) clearance?

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

Who is the listed applicant for Socrates 38 Catheter?

The FDA 510(k) record lists Scientia Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Socrates 38 Catheter?

The FDA product code for Socrates 38 Catheter is QJP.

Other records listing Scientia Vascular, 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.

View all 17 devices →

Related Devices (Code: QJP)

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.