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FDA 510(k)

MODEL 750E SERIES MONITOR

K-Number: K051896 · 2005-12-16

ApplicantCas Medical Systems, Inc.
Decision Date2005-12-16
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 750E SERIES MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Cas Medical Systems, Inc.. It received FDA 510(k) clearance on 2005-12-16 under 510(k) number K051896. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 750E SERIES MONITOR?

MODEL 750E SERIES MONITOR is a medical device that received FDA 510(k) clearance on 2005-12-16. The listed applicant is Cas Medical Systems, Inc.. The 510(k) number is K051896.

When did MODEL 750E SERIES MONITOR receive FDA 510(k) clearance?

MODEL 750E SERIES MONITOR received FDA 510(k) clearance on 2005-12-16, under 510(k) number K051896.

Who is the listed applicant for MODEL 750E SERIES MONITOR?

The FDA 510(k) record lists Cas Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 750E SERIES MONITOR?

The FDA product code for MODEL 750E SERIES MONITOR is MWI.

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Related Devices (Code: MWI)

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.

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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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