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FDA 510(k)

A-VIEW BASIC AND PLUS

K-Number: K070515 · 2007-07-30

ApplicantCordatec N.V.
Decision Date2007-07-30
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

A-VIEW BASIC AND PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Cordatec N.V.. It received FDA 510(k) clearance on 2007-07-30 under 510(k) number K070515. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-VIEW BASIC AND PLUS?

A-VIEW BASIC AND PLUS is a medical device that received FDA 510(k) clearance on 2007-07-30. The listed applicant is Cordatec N.V.. The 510(k) number is K070515.

When did A-VIEW BASIC AND PLUS receive FDA 510(k) clearance?

A-VIEW BASIC AND PLUS received FDA 510(k) clearance on 2007-07-30, under 510(k) number K070515.

Who is the listed applicant for A-VIEW BASIC AND PLUS?

The FDA 510(k) record lists Cordatec N.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A-VIEW BASIC AND PLUS?

The FDA product code for A-VIEW BASIC AND PLUS is ITX.

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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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