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FDA 510(k)

VILET VILET QUICK

K-Number: K120556 · 2012-05-23

ApplicantRiverpoint Medical
Decision Date2012-05-23
Product CodeGAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VILET VILET QUICK is the device name listed in this FDA 510(k) record. The listed applicant is Riverpoint Medical. It received FDA 510(k) clearance on 2012-05-23 under 510(k) number K120556. The device is classified under product code GAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VILET VILET QUICK?

VILET VILET QUICK is a medical device that received FDA 510(k) clearance on 2012-05-23. The listed applicant is Riverpoint Medical. The 510(k) number is K120556.

When did VILET VILET QUICK receive FDA 510(k) clearance?

VILET VILET QUICK received FDA 510(k) clearance on 2012-05-23, under 510(k) number K120556.

Who is the listed applicant for VILET VILET QUICK?

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

What is the FDA product code for VILET VILET QUICK?

The FDA product code for VILET VILET QUICK is GAM.

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Other records listing Riverpoint Medical as applicant

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Related Devices (Code: GAM)

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.

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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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