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FDA 510(k)

VUSION CS PLUS

K-Number: K122588 · 2013-06-12

ApplicantOrtho Development Corp.
Decision Date2013-06-12
Product CodeODP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VUSION CS PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Development Corp.. It received FDA 510(k) clearance on 2013-06-12 under 510(k) number K122588. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VUSION CS PLUS?

VUSION CS PLUS is a medical device that received FDA 510(k) clearance on 2013-06-12. The listed applicant is Ortho Development Corp.. The 510(k) number is K122588.

When did VUSION CS PLUS receive FDA 510(k) clearance?

VUSION CS PLUS received FDA 510(k) clearance on 2013-06-12, under 510(k) number K122588.

Who is the listed applicant for VUSION CS PLUS?

The FDA 510(k) record lists Ortho Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VUSION CS PLUS?

The FDA product code for VUSION CS PLUS is ODP.

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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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