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FDA 510(k)

Well-Root ST

K-Number: K170950 · 2017-12-20

Decision Date2017-12-20
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Well-Root ST 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 2017-12-20 under 510(k) number K170950. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Well-Root ST?

Well-Root ST is a medical device that received FDA 510(k) clearance on 2017-12-20. The listed applicant is Vericom Co., Ltd.. The 510(k) number is K170950.

When did Well-Root ST receive FDA 510(k) clearance?

Well-Root ST received FDA 510(k) clearance on 2017-12-20, under 510(k) number K170950.

Who is the listed applicant for Well-Root ST?

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 Well-Root ST?

The FDA product code for Well-Root ST is KIF.

Other records listing Vericom Co., Ltd. as applicant

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.

View all 8 devices →

Related Devices (Code: KIF)

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.

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.