Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015181391

FEI Number

3015181391

Entity Name

Murata Vios, Private Limited

City/State/Country

Kodihalli, Bangalore Karnataka, IN

Establishment Address

Prestige Sterling Square, No.204, 3rd Floor, Wing-A, 3, Madras Bank Road, Off Lavelle Road, Kodihalli, Bangalore Karnataka 560001, IN

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device,Remanufacture Medical Device

Owner / Operator

Murata Vios, Inc. (Owner Number: 10059850)

Owner / Operator Contact Address

700 Commerce Drive, Suite 190, Woodbury, MN 55125, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K172586

PMA Number

N/A

All Registered Proprietary Names

Vios Central Station Monitor/Vios Central Server Software 2050 Vios Monitoring System Model 2050

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OUG	Medical Device Data System	General Hospital	Class 1	880.6310	2019-02-28
DXJ	Display, Cathode-Ray Tube, Medical	Cardiovascular	Class 2	870.2450	2019-02-28
DRT	Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)	Cardiovascular	Class 2	870.2300	2019-02-28
DPZ	Oximeter, Ear	Cardiovascular	Class 2	870.2710	2019-02-28
DRG	Transmitters And Receivers, Physiological Signal, Radiofrequency	Cardiovascular	Class 2	870.2910	2019-02-28
DQA	Oximeter	Cardiovascular	Class 2	870.2700	2019-02-28

Official Correspondent

No official correspondent registered.

US Agent Details

John Lansdown Business: VIOS MEDICAL, A MURATA COMPANY Email: john.lansdown@murata.com Phone: (651) 8888125

Related Public Records

Same Entity

Murata Vios, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3015328411	Murata Vios, Inc.	Woodbury, MN, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K180534	Philips Medizin Systeme Boeblingen GmbH	Philips IntelliVue GuardianSoftware	2018-07-16
K161767	Philips Medizin Systeme Boeblingen GmbH	Philips IntelliVue GuardianSoftware	2017-01-27
K212208	Philips Medizin Systeme Boeblingen GmbH	Philips IntelliVue GuardianSoftware (Rev. E.0X)	2021-09-30
K832250	Litton Medical Electronics	SERVOMED BASIC BEDSIDE UNIT SMA 102-	1984-06-01
K801515	Abbott Medical Electronics Co.	ABBY II PATIENT MONITOR OR VITAL SIGNS M	1980-07-08

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0020-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20 (US) N, Part Number CS08651
Z-0022-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02
Z-0023-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-03
Z-0028-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	Capnostream20 (US) M, Part Number CS08653
Z-0029-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	Capnostream20 (US) M W/PRINTER, Part Number CS08659

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015181391. Last updated year: 2026. Please use registration number 3015181391 when referencing this establishment in official correspondence.