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FDA 510(k)

VONFLEX HEAVY, VINFLEX LIGHT

K-Number: K103164 · 2010-11-10

ApplicantVericom Co., Ltd.
Decision Date2010-11-10
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VONFLEX HEAVY, VINFLEX LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Vericom Co., Ltd.. It received FDA 510(k) clearance on 2010-11-10 under 510(k) number K103164. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VONFLEX HEAVY, VINFLEX LIGHT?

VONFLEX HEAVY, VINFLEX LIGHT is a medical device that received FDA 510(k) clearance on 2010-11-10. The listed applicant is Vericom Co., Ltd.. The 510(k) number is K103164.

When did VONFLEX HEAVY, VINFLEX LIGHT receive FDA 510(k) clearance?

VONFLEX HEAVY, VINFLEX LIGHT received FDA 510(k) clearance on 2010-11-10, under 510(k) number K103164.

Who is the listed applicant for VONFLEX HEAVY, VINFLEX LIGHT?

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

What is the FDA product code for VONFLEX HEAVY, VINFLEX LIGHT?

The FDA product code for VONFLEX HEAVY, VINFLEX LIGHT is ELW.

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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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