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FDA 510(k)

740 SELECT

K-Number: K130411 · 2013-05-29

ApplicantCas Medical Systems, Inc.
Decision Date2013-05-29
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

740 SELECT 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 2013-05-29 under 510(k) number K130411. 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 740 SELECT?

740 SELECT is a medical device that received FDA 510(k) clearance on 2013-05-29. The listed applicant is Cas Medical Systems, Inc.. The 510(k) number is K130411.

When did 740 SELECT receive FDA 510(k) clearance?

740 SELECT received FDA 510(k) clearance on 2013-05-29, under 510(k) number K130411.

Who is the listed applicant for 740 SELECT?

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 740 SELECT?

The FDA product code for 740 SELECT is MWI.

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Related Devices (Code: MWI)

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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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