FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Socrates Aspiration System

K Number: K223913 · Decision Sep 20, 2023
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
108
Applicant Total
7
Review Days
265

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Socrates Aspiration System
K Number
K223913
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Scientia Vascular, Inc.
Date Received
December 29, 2022
Decision Date
September 20, 2023
Product Code
NRY
Advisory Committee
Cardiovascular
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NRY Catheter, Thrombus Retriever

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NRY), ordered by most recent decision date.

View all

Other Clearances by Scientia Vascular, Inc.

K Number Device Name
K253579 Aristotle 14 Guidewire; Aristotle 18 Guidewire; Aristotle 24 Guidewire; Zoom Wire 14 Guidewire
K243938 Aristotle 14 Guidewire; Aristotle 18 Guidewire; Aristotle 24 Guidewire; Zoom Wire 14 Guidewire; Aristotle Colossus Guidewire
K242301 Socrates 38 Catheter
K223560 Plato 17 Microcatheter
K231954 Aristotle 18 Guidewire; Aristotle 24 Guidewire
K222437 Aristotle Colossus Guidewire