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FDA 510(k)

PATIENT MONITOR, MODELS DASH 3000, 4000 AND 5000

K-Number: K051367 · 2005-06-20

Decision Date2005-06-20
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATIENT MONITOR, MODELS DASH 3000, 4000 AND 5000 is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Information Technologies. It received FDA 510(k) clearance on 2005-06-20 under 510(k) number K051367. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 136 devices →

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

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

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