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FDA 510(k)

CONNEXALL SUITE OF SOFTWARE PRODUCTS

K-Number: K112650 · 2012-02-01

ApplicantConnexall USA, Inc.
Decision Date2012-02-01
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONNEXALL SUITE OF SOFTWARE PRODUCTS is the device name listed in this FDA 510(k) record. The listed applicant is Connexall USA, Inc.. It received FDA 510(k) clearance on 2012-02-01 under 510(k) number K112650. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONNEXALL SUITE OF SOFTWARE PRODUCTS?

CONNEXALL SUITE OF SOFTWARE PRODUCTS is a medical device that received FDA 510(k) clearance on 2012-02-01. The listed applicant is Connexall USA, Inc.. The 510(k) number is K112650.

When did CONNEXALL SUITE OF SOFTWARE PRODUCTS receive FDA 510(k) clearance?

CONNEXALL SUITE OF SOFTWARE PRODUCTS received FDA 510(k) clearance on 2012-02-01, under 510(k) number K112650.

Who is the listed applicant for CONNEXALL SUITE OF SOFTWARE PRODUCTS?

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

What is the FDA product code for CONNEXALL SUITE OF SOFTWARE PRODUCTS?

The FDA product code for CONNEXALL SUITE OF SOFTWARE PRODUCTS is MSX.

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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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