Impact (Informing Mobile Personnel and Care Tracking) Pager System

FDA 510(k) K971868 · Marquette Electronics, Inc.

Substantially Equivalent

510(k) numberK971868

Submission

Device name
Impact (Informing Mobile Personnel and Care Tracking) Pager System
Applicant
Marquette Electronics, Inc.
Milwaukee, WI, US
Received
May 20, 1997
Decision date
November 13, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MSX – System, Network And Communication, Physiological Monitors
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2300
Specialty
Cardiovascular
Life-sustaining
Yes

Other 510(k)s with product code MSX

510(k)DeviceApplicantDecision
K261287Digistat CareMSX · Traditional Ascom Ums Srl Unipersonale09/12/2026SE
K260211Dashboard (P007000)MSX · Traditional Hill-Rom, Inc.08/13/2026SE
K261367Corsano CardioWatch 287-2 SystemMSX · Traditional Corsano Health B.V.07/26/2026SE
K253654IntelliVue Measurement Rack 6000 (867317)MSX · Traditional Philips Medizin Systeme Böblingen GmbH03/30/2026SE
K243270TigerConnect Alarm ManagementMSX · Traditional Tigerconnect09/30/2025SE
K242728BeneVision Central Monitoring SystemMSX · Traditional Shenzhen Mindray Bio-Medical Electronics Co., Ltd.07/31/2025SE
K242750Central StationMSX · Traditional Nihon Kohden Digital Health Solutions, LLC06/05/2025SE
K242842ANNE View, Central HubMSX · Traditional Sibel Health, Inc.01/08/2025SE
K241397HinscopeMSX · Traditional Hinlab Sas11/14/2024SE
K233834Infinity Gateway SuiteMSX · Traditional Draeger Medical Systems, Inc.07/12/2024SE

More from Draeger Medical Systems, Inc.

510(k)DeviceDecision
K971683Wireless Lan (Local Area Network) - Wireless EthernetMSX · Traditional 10/22/1997SE
K972199Signal-Averaged High Resolution P Wave AnalysisDPS · Traditional 09/25/1997SE
K962547Cardioserv PDRO · Traditional 03/06/1997SE
K963120Responder 2500 Defibrillator and Cardiac Care SystemDRO · Traditional 02/28/1997SE
K962827Alarm Display Unit/Pager-Lan System (Adu)DSI · Traditional 02/24/1997SE
K964750Eagle 4000 Patient MonitorLOS · Traditional 02/21/1997SE
K962551Cardioserv SLDD · Traditional 11/19/1996ST
K960418Eagle Patient MonitorDSI · Traditional 10/02/1996SE
K960272Eagle 3000/3100 Patient MonitorMLD · Traditional 10/02/1996SE
K961139Eagle Patient Monitor Model 3000/3100DSI · Traditional 08/09/1996SE

Questions and answers

When was Impact (Informing Mobile Personnel and Care Tracking) Pager System cleared by the FDA?

Impact (Informing Mobile Personnel and Care Tracking) Pager System (K971868) received a 510(k) decision of Substantially Equivalent on November 13, 1997, 177 days after the submission was received.

What is the product code of K971868?

The FDA product code is MSX – System, Network And Communication, Physiological Monitors, a Class II (moderate risk) device regulated under 21 CFR 870.2300.