MDP2000 Medical Data Processor

FDA 510(k) K972880 · Vidco, Inc.

Substantially Equivalent

510(k) numberK972880

Submission

Device name
MDP2000 Medical Data Processor
Applicant
Vidco, Inc.
Beaverton, OR, US
Received
August 5, 1997
Decision date
October 22, 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
K934093580CDR Display DriverDXJ · Traditional 08/18/1994SE
K932894620CSR Display DriverDXJ · Traditional 06/20/1994SE
K926298520 Display Driver- Status IDRT · Traditional 05/04/1994SE
K926219516YT Display DriverDXJ · Traditional 12/16/1993SE
K926162580CD Display DriverDXJ · Traditional 11/08/1993SE
K890353SMDS460 Surgical Monitor Display SystemDXJ · Traditional 03/02/1989SE

Questions and answers

When was MDP2000 Medical Data Processor cleared by the FDA?

MDP2000 Medical Data Processor (K972880) received a 510(k) decision of Substantially Equivalent on October 22, 1997, 78 days after the submission was received.

What is the product code of K972880?

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