Vitalert 2000 Vital Signs Monitor

FDA 510(k) K882031 · Draeger Medical, Inc.

Substantially Equivalent

510(k) numberK882031

Submission

Device name
Vitalert 2000 Vital Signs Monitor
Applicant
Draeger Medical, Inc.
Telford, PA, US
Received
May 16, 1988
Decision date
July 28, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DXO – Transducer, Pressure, Catheter Tip
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2870
Specialty
Cardiovascular

Other 510(k)s with product code DXO

510(k)DeviceApplicantDecision
K251367OptoMonitor 3DXO · Traditional Opsens, Inc.01/16/2026SE
K241418OptoMonitor 3DXO · Traditional Opsens, Inc.02/12/2025SE
K233904ACIST RXi System (016616); ACIST Navvus II Catheter (016675_DXO · Traditional Acist Medical Systems, Inc.07/17/2024SE
K222216TruWave Disposable Pressure TransducerDXO · Traditional Edwards Lifesciences, LLC12/22/2022SE
K202943OptoMonitor 3DXO · Traditional Opsens, Inc.11/24/2020SE
K193620OptoMonitor 3DXO · Traditional Opsens, Inc.06/18/2020SE
K193279Comet II Pressure GuidewireDXO · Special Boston Scientific Corporation12/23/2019SE
K192340OptoMonitorDXO · Traditional Opsens, Inc.12/12/2019SE
K190852Zurich Pressure Guidewire System Model 100DXO · Traditional Zurich Medical, Inc.08/14/2019SE
K183413TruWave Disposable Pressure TransducerDXO · Traditional Edwards Lifeciences, LLC05/01/2019SE

More from Edwards Lifeciences, LLC

510(k)DeviceDecision
K121886Savina 300 Savina 300, Country VariantsCBK · Traditional 08/08/2014SE
K133886Perseus A500BSZ · Traditional 06/20/2014SE
K121999General Purpose Temperature Probe, Skin Temperature ProbeFLL · Traditional 02/28/2013SE
K103035Smartpilot View Model MK04500BSZ · Traditional 03/28/2012SE
K102618Ventstar Heated, Infinity Id Breathing Circuit HeatedBTT · Traditional 12/10/2010SE
K092029Ventstar Resuscitaire, Model MP00311, Ventstar Resuscitaire Ceu, Model MP00310BYE · Traditional 08/06/2010SE
K100941Infinity Mcable - Mainstream CO2CCK · Special 04/23/2010SE
K092999NBP CuffDXQ · Traditional 11/24/2009SE
K083050Evite XLCBK · Special 12/29/2008SE
K081447Fourth Gas Module with CO2 for Primus US ApolloBSZ · Traditional 10/08/2008SE

Questions and answers

When was Vitalert 2000 Vital Signs Monitor cleared by the FDA?

Vitalert 2000 Vital Signs Monitor (K882031) received a 510(k) decision of Substantially Equivalent on July 28, 1988, 73 days after the submission was received.

What is the product code of K882031?

The FDA product code is DXO – Transducer, Pressure, Catheter Tip, a Class II (moderate risk) device regulated under 21 CFR 870.2870.