PATIENTNET MONITORING SYSTEM
K-Number: K020524 · 2002-03-20
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Device Summary
Frequently Asked Questions
What is the PATIENTNET MONITORING SYSTEM?
PATIENTNET MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2002-03-20. The listed applicant is General Electric Medical Systems Information Techn. The 510(k) number is K020524.
When did PATIENTNET MONITORING SYSTEM receive FDA 510(k) clearance?
PATIENTNET MONITORING SYSTEM received FDA 510(k) clearance on 2002-03-20, under 510(k) number K020524.
Who is the listed applicant for PATIENTNET MONITORING SYSTEM?
The FDA 510(k) record lists General Electric Medical Systems Information Techn as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENTNET MONITORING SYSTEM?
The FDA product code for PATIENTNET MONITORING SYSTEM is MSX.
Related Clinical Trials
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.
Other records listing General Electric Medical Systems Information Techn 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.
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.
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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