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FDA 510(k)

Bidop 7

K-Number: K201114 · 2021-01-05

ApplicantKoven Technology, Inc.
Decision Date2021-01-05
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Bidop 7 is a medical device manufactured by Koven Technology, Inc.. It received FDA 510(k) clearance on 2021-01-05 under approval number K201114. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Bidop 7?

Bidop 7 is a medical device that received FDA 510(k) clearance on 2021-01-05. It is manufactured by Koven Technology, Inc.. The 510(k) number is K201114.

When was Bidop 7 approved by the FDA?

Bidop 7 received FDA 510(k) clearance on 2021-01-05, under approval number K201114.

What company makes Bidop 7?

Bidop 7 is manufactured by Koven Technology, Inc..

What is the FDA product code for Bidop 7?

The FDA product code for Bidop 7 is DPW.

Other Devices by Koven Technology, Inc.

K153762Smartdop XT6

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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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