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CASSIE

by Wesper, Inc.

510(k) K252628

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK252628 Date27 Apr 2026ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
MNR
Device Class
Class II
Regulation
21 CFR Part 868.2375
Advisory Committee
Anesthesiology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 23 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The CASSIE is a Ventilatory Effort Recorder classified under device class 2. It is designed to record ventilatory effort as part of respiratory monitoring.

The device received FDA 510(k) clearance (K252628) on April 27, 2026, and is manufactured by Wesper, Inc. It is intended for use in anesthesiology settings and is supplied as a non-sterile, reusable device. Storage and handling should follow standard conditions for electronic monitoring equipment.

Other devices from Wesper, Inc.