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FDA 510(k)

FiteBac Cavity Cleanser

K-Number: K190271 · 2020-01-23

ApplicantLargent Health, LLC
Decision Date2020-01-23
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FiteBac Cavity Cleanser is a medical device manufactured by Largent Health, LLC. It received FDA 510(k) clearance on 2020-01-23 under approval number K190271. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FiteBac Cavity Cleanser?

FiteBac Cavity Cleanser is a medical device that received FDA 510(k) clearance on 2020-01-23. It is manufactured by Largent Health, LLC. The 510(k) number is K190271.

When was FiteBac Cavity Cleanser approved by the FDA?

FiteBac Cavity Cleanser received FDA 510(k) clearance on 2020-01-23, under approval number K190271.

What company makes FiteBac Cavity Cleanser?

FiteBac Cavity Cleanser is manufactured by Largent Health, LLC.

What is the FDA product code for FiteBac Cavity Cleanser?

The FDA product code for FiteBac Cavity Cleanser is LBH.

Other Devices by Largent Health, LLC

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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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