meddevicedb.com FDA Device Reference

Asurys Fluid Management System

K251273 Class II Traditional
Decision Date
2026-03-27
Sponsor / Applicant
Boston Scientific Corporation

Technical Specification

510(k) Submission ID K251273
Product Code HIG
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1700
Decision Date 2026-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Asurys Fluid Management System received FDA 510(k) clearance under submission number K251273, sponsored by Boston Scientific Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2026-03-27.

Classification & Regulation

This clearance is catalogued under FDA product code HIG and 21 CFR 884.1700, within the Obstetrics/Gynecology review panel as a Class II device.