FDA 510(k)

Avid CT2

K-Number: K202490 · 2020-11-16

ApplicantVision Quest Industries Inc./Dba VQ Orthocare

Decision Date2020-11-16

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Avid CT2 is the device name listed in this FDA 510(k) record. The listed applicant is Vision Quest Industries Inc./Dba VQ Orthocare. It received FDA 510(k) clearance on 2020-11-16 under 510(k) number K202490. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Avid CT2?

Avid CT2 is a medical device that received FDA 510(k) clearance on 2020-11-16. The listed applicant is Vision Quest Industries Inc./Dba VQ Orthocare. The 510(k) number is K202490.

When did Avid CT2 receive FDA 510(k) clearance?

Avid CT2 received FDA 510(k) clearance on 2020-11-16, under 510(k) number K202490.

Who is the listed applicant for Avid CT2?

The FDA 510(k) record lists Vision Quest Industries Inc./Dba VQ Orthocare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Avid CT2?

The FDA product code for Avid CT2 is IPF.

Other records listing Vision Quest Industries Inc./Dba VQ Orthocare as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K183692Avid IF2

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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.