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FDA 510(k)

Socrates Aspiration System (Socrates 70 Aspiration Catheter)

K-Number: K260002 · 2026-07-16

ApplicantScientia Vascular, Inc.
Decision Date2026-07-16
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Socrates Aspiration System (Socrates 70 Aspiration 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 2026-07-16 under 510(k) number K260002. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Socrates Aspiration System (Socrates 70 Aspiration Catheter)?

Socrates Aspiration System (Socrates 70 Aspiration Catheter) is a medical device that received FDA 510(k) clearance on 2026-07-16. The listed applicant is Scientia Vascular, Inc.. The 510(k) number is K260002.

When did Socrates Aspiration System (Socrates 70 Aspiration Catheter) receive FDA 510(k) clearance?

Socrates Aspiration System (Socrates 70 Aspiration Catheter) received FDA 510(k) clearance on 2026-07-16, under 510(k) number K260002.

Who is the listed applicant for Socrates Aspiration System (Socrates 70 Aspiration 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 Aspiration System (Socrates 70 Aspiration Catheter)?

The FDA product code for Socrates Aspiration System (Socrates 70 Aspiration Catheter) is NRY.

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.

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Related Devices (Code: NRY)

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.

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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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