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FDA 510(k)

VERGE VIDEOMETER

K-Number: K962148 · 1996-12-20

ApplicantVerg, Inc.
Decision Date1996-12-20
Product CodeFXN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VERGE VIDEOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Verg, Inc.. It received FDA 510(k) clearance on 1996-12-20 under 510(k) number K962148. The device is classified under product code FXN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERGE VIDEOMETER?

VERGE VIDEOMETER is a medical device that received FDA 510(k) clearance on 1996-12-20. The listed applicant is Verg, Inc.. The 510(k) number is K962148.

When did VERGE VIDEOMETER receive FDA 510(k) clearance?

VERGE VIDEOMETER received FDA 510(k) clearance on 1996-12-20, under 510(k) number K962148.

Who is the listed applicant for VERGE VIDEOMETER?

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

What is the FDA product code for VERGE VIDEOMETER?

The FDA product code for VERGE VIDEOMETER is FXN.

Related Clinical Trials

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Related Devices (Code: FXN)

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.

K131596WOUND MEASURING & MONITORING DEVICEWoundvision, LLCK130165PICTZAR DIGITAL PLANIMETRY SOFTWARE APPLICATION 7.0Advanced Planimetric Services, LLCK070426SILHOUETTE, MODEL 1000.01Aranz Medical Limited

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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