Asurys Fluid Management System

FDA 510(k) K251273 · Boston Scientific Corporation

Substantially Equivalent

510(k) numberK251273

Submission

Device name
Asurys Fluid Management System
Applicant
Boston Scientific Corporation
Marborough, MA, US
Received
April 24, 2025
Decision date
March 27, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HIG – Insufflator, Hysteroscopic
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1700
Specialty
Obstetrics/Gynecology

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Questions and answers

When was Asurys Fluid Management System cleared by the FDA?

Asurys Fluid Management System (K251273) received a 510(k) decision of Substantially Equivalent on March 27, 2026, 337 days after the submission was received.

What is the product code of K251273?

The FDA product code is HIG – Insufflator, Hysteroscopic, a Class II (moderate risk) device regulated under 21 CFR 884.1700.