ClearanceBrief
Company ยท US

Etiometry, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2015 to 2026. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MWIMonitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)5
PPWAdjunctive Cardiovascular Status Indicator4
PLBMultivariate Vital Signs Index2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 3, 2026K254066Etiometry Platform
Etiometry, Inc.
PPW
Feb 12, 2025K241479Etiometry Platform (DAV 5.4 RAE 9.2)
Etiometry, Inc.
PPW
Jul 7, 2023K223578T3 Platform software
Etiometry, Inc.
PPW
Jan 6, 2023K213423T3 Platform software
Etiometry, Inc.
PLB
Jun 22, 2022K213230T3 Platform Software
Etiometry, Inc.
PPW
Nov 25, 2020K202306T3 Platform software
Etiometry, Inc.
MWI
Dec 8, 2019K190273T3 Platform software
Etiometry, Inc.
MWI
May 26, 2017K163065T3 Software
Etiometry, Inc.
MWI
Mar 31, 2016K152258T3 Software
Etiometry, Inc.
PLB
Oct 29, 2015K151715T3 Software
Etiometry, Inc.
MWI
Mar 4, 2015K142732T3 Software
Etiometry, Inc.
MWI

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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