UNITY NETWORK PATIENT DATA SERVER
K-Number: K032582 · 2003-09-17
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Device Summary
Frequently Asked Questions
What is the UNITY NETWORK PATIENT DATA SERVER?
UNITY NETWORK PATIENT DATA SERVER is a medical device that received FDA 510(k) clearance on 2003-09-17. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K032582.
When did UNITY NETWORK PATIENT DATA SERVER receive FDA 510(k) clearance?
UNITY NETWORK PATIENT DATA SERVER received FDA 510(k) clearance on 2003-09-17, under 510(k) number K032582.
Who is the listed applicant for UNITY NETWORK PATIENT DATA SERVER?
The FDA 510(k) record lists Ge Medical Systems Information Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNITY NETWORK PATIENT DATA SERVER?
The FDA product code for UNITY NETWORK PATIENT DATA SERVER 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 Ge Medical Systems Information Technologies 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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