PATIENT MONITOR, MODELS DASH 3000, 4000 AND 5000
K-Number: K051367 · 2005-06-20
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Device Summary
Frequently Asked Questions
What is the PATIENT MONITOR, MODELS DASH 3000, 4000 AND 5000?
PATIENT MONITOR, MODELS DASH 3000, 4000 AND 5000 is a medical device that received FDA 510(k) clearance on 2005-06-20. The listed applicant is Ge Medical Systems Information Technologies. The 510(k) number is K051367.
When did PATIENT MONITOR, MODELS DASH 3000, 4000 AND 5000 receive FDA 510(k) clearance?
PATIENT MONITOR, MODELS DASH 3000, 4000 AND 5000 received FDA 510(k) clearance on 2005-06-20, under 510(k) number K051367.
Who is the listed applicant for PATIENT MONITOR, MODELS DASH 3000, 4000 AND 5000?
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 PATIENT MONITOR, MODELS DASH 3000, 4000 AND 5000?
The FDA product code for PATIENT MONITOR, MODELS DASH 3000, 4000 AND 5000 is MHX.
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: MHX)
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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