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FDA 510(k)

MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM

K-Number: K013156 · 2001-10-19

ApplicantData Critical Corp.
Decision Date2001-10-19
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Data Critical Corp.. It received FDA 510(k) clearance on 2001-10-19 under 510(k) number K013156. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM?

MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM is a medical device that received FDA 510(k) clearance on 2001-10-19. The listed applicant is Data Critical Corp.. The 510(k) number is K013156.

When did MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM received FDA 510(k) clearance on 2001-10-19, under 510(k) number K013156.

Who is the listed applicant for MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM?

The FDA 510(k) record lists Data Critical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM?

The FDA product code for MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM is MSX.

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Other records listing Data Critical Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K012005MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEMK011999MODIFICATION TO FLEXVIEW CLINICAL MONITORING SYSTEMK010912ALARMVIEW WIRELESS DATA NETWORK SYSTEMK003998FLEXVIEW CLINICAL MONITORING SYSTEMK992848ALARMVIEW SYSTEMK990378STATVIEW SYSTEM

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Related Devices (Code: MSX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261287Digistat CareAscom Ums Srl UnipersonaleK260211Dashboard (P007000)Hill-Rom, Inc.K261367Corsano CardioWatch 287-2 SystemCorsano Health B.V.K253654IntelliVue Measurement Rack 6000 (867317)Philips Medizin Systeme Böblingen GmbHK243270TigerConnect Alarm ManagementTigerconnectK242728BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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