Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VTS1000

K-Number: K101838 · 2011-02-18

ApplicantVuetek Scientific, LLC
Decision Date2011-02-18
Product CodeKZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VTS1000 is the device name listed in this FDA 510(k) record. The listed applicant is Vuetek Scientific, LLC. It received FDA 510(k) clearance on 2011-02-18 under 510(k) number K101838. The device is classified under product code KZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VTS1000?

VTS1000 is a medical device that received FDA 510(k) clearance on 2011-02-18. The listed applicant is Vuetek Scientific, LLC. The 510(k) number is K101838.

When did VTS1000 receive FDA 510(k) clearance?

VTS1000 received FDA 510(k) clearance on 2011-02-18, under 510(k) number K101838.

Who is the listed applicant for VTS1000?

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

What is the FDA product code for VTS1000?

The FDA product code for VTS1000 is KZA.

Related Devices (Code: KZA)

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.

K152088IV-eyeNovarix LimitedK042679IR VIEWERInfrared Imaging Systems, Inc.K982612ESP7 VENOUS IMAGEIronmaster, Inc.K780884HYPO-GRIPHarco ProductsK780883E-Z-JECTORHarco Products

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.

↑