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FDA 510(k)

VECTTOR VT-200

K-Number: K121662 · 2012-11-21

ApplicantAlan Neuromedical Technologies, LLC
Decision Date2012-11-21
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VECTTOR VT-200 is the device name listed in this FDA 510(k) record. The listed applicant is Alan Neuromedical Technologies, LLC. It received FDA 510(k) clearance on 2012-11-21 under 510(k) number K121662. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTTOR VT-200?

VECTTOR VT-200 is a medical device that received FDA 510(k) clearance on 2012-11-21. The listed applicant is Alan Neuromedical Technologies, LLC. The 510(k) number is K121662.

When did VECTTOR VT-200 receive FDA 510(k) clearance?

VECTTOR VT-200 received FDA 510(k) clearance on 2012-11-21, under 510(k) number K121662.

Who is the listed applicant for VECTTOR VT-200?

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

What is the FDA product code for VECTTOR VT-200?

The FDA product code for VECTTOR VT-200 is LIH.

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Related Devices (Code: LIH)

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.

K231575Vecttor VT-300Artaflex, Inc.K202725ETD4000Therasigma, LLCK183692Avid IF2Vision Quest Industries Inc./Dba VQ OrthocareK122944GEMORE TRUE SINE INTERFERENTIAL STIMULATORGemore Technology Co, Ltd.K110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908Everyway Medical Instruments Co.,LtdK100246MAX-IF1000Bio Protech, Inc.

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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