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FDA 510(k)

THE VISONIC DOME(TM)

K-Number: K902306 · 1990-12-21

ApplicantVista Vision
Decision Date1990-12-21
Product CodeLYL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE VISONIC DOME(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Vista Vision. It received FDA 510(k) clearance on 1990-12-21 under 510(k) number K902306. The device is classified under product code LYL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE VISONIC DOME(TM)?

THE VISONIC DOME(TM) is a medical device that received FDA 510(k) clearance on 1990-12-21. The listed applicant is Vista Vision. The 510(k) number is K902306.

When did THE VISONIC DOME(TM) receive FDA 510(k) clearance?

THE VISONIC DOME(TM) received FDA 510(k) clearance on 1990-12-21, under 510(k) number K902306.

Who is the listed applicant for THE VISONIC DOME(TM)?

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

What is the FDA product code for THE VISONIC DOME(TM)?

The FDA product code for THE VISONIC DOME(TM) is LYL.

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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.

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