FDA 510(k)

VITELCARE TURTLE, MODEL 400

K-Number: K043368 · 2005-02-01

ApplicantVisual Telecommunications Network, Inc.

Decision Date2005-02-01

Product CodeMWI

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

VITELCARE TURTLE, MODEL 400 is the device name listed in this FDA 510(k) record. The listed applicant is Visual Telecommunications Network, Inc.. It received FDA 510(k) clearance on 2005-02-01 under 510(k) number K043368. 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 VITELCARE TURTLE, MODEL 400?

VITELCARE TURTLE, MODEL 400 is a medical device that received FDA 510(k) clearance on 2005-02-01. The listed applicant is Visual Telecommunications Network, Inc.. The 510(k) number is K043368.

When did VITELCARE TURTLE, MODEL 400 receive FDA 510(k) clearance?

VITELCARE TURTLE, MODEL 400 received FDA 510(k) clearance on 2005-02-01, under 510(k) number K043368.

Who is the listed applicant for VITELCARE TURTLE, MODEL 400?

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

What is the FDA product code for VITELCARE TURTLE, MODEL 400?

The FDA product code for VITELCARE TURTLE, MODEL 400 is MWI.

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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.