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FDA 510(k)

VERT-X UNIVERSAL VERTICAL BUCKY STAND

K-Number: K922443 · 1992-10-26

Decision Date1992-10-26
Product CodeIXY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VERT-X UNIVERSAL VERTICAL BUCKY STAND is the device name listed in this FDA 510(k) record. The listed applicant is Afp Imaging Corp.. It received FDA 510(k) clearance on 1992-10-26 under 510(k) number K922443. The device is classified under product code IXY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERT-X UNIVERSAL VERTICAL BUCKY STAND?

VERT-X UNIVERSAL VERTICAL BUCKY STAND is a medical device that received FDA 510(k) clearance on 1992-10-26. The listed applicant is Afp Imaging Corp.. The 510(k) number is K922443.

When did VERT-X UNIVERSAL VERTICAL BUCKY STAND receive FDA 510(k) clearance?

VERT-X UNIVERSAL VERTICAL BUCKY STAND received FDA 510(k) clearance on 1992-10-26, under 510(k) number K922443.

Who is the listed applicant for VERT-X UNIVERSAL VERTICAL BUCKY STAND?

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

What is the FDA product code for VERT-X UNIVERSAL VERTICAL BUCKY STAND?

The FDA product code for VERT-X UNIVERSAL VERTICAL BUCKY STAND is IXY.

Related Clinical Trials

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.

Other records listing Afp Imaging Corp. 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.

View all 13 devices →

Related Devices (Code: IXY)

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.

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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