FDA 510(k)

Avid IF2

K-Number: K183692 · 2019-06-12

ApplicantVision Quest Industries Inc./Dba VQ Orthocare

Decision Date2019-06-12

Product CodeLIH

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Avid IF2 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 2019-06-12 under 510(k) number K183692. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Avid IF2?

Avid IF2 is a medical device that received FDA 510(k) clearance on 2019-06-12. The listed applicant is Vision Quest Industries Inc./Dba VQ Orthocare. The 510(k) number is K183692.

When did Avid IF2 receive FDA 510(k) clearance?

Avid IF2 received FDA 510(k) clearance on 2019-06-12, under 510(k) number K183692.

Who is the listed applicant for Avid IF2?

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 IF2?

The FDA product code for Avid IF2 is LIH.

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.

K202490Avid CT2

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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.