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FDA 510(k)

V QUICK PATCH

K-Number: K993934 · 2000-08-15

ApplicantVq Corp.
Decision Date2000-08-15
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

V QUICK PATCH is the device name listed in this FDA 510(k) record. The listed applicant is Vq Corp.. It received FDA 510(k) clearance on 2000-08-15 under 510(k) number K993934. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V QUICK PATCH?

V QUICK PATCH is a medical device that received FDA 510(k) clearance on 2000-08-15. The listed applicant is Vq Corp.. The 510(k) number is K993934.

When did V QUICK PATCH receive FDA 510(k) clearance?

V QUICK PATCH received FDA 510(k) clearance on 2000-08-15, under 510(k) number K993934.

Who is the listed applicant for V QUICK PATCH?

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

What is the FDA product code for V QUICK PATCH?

The FDA product code for V QUICK PATCH is DRX.

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Related Devices (Code: DRX)

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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