TAP Lancet
K-Number: K223201 · 2023-04-19
ApplicantYourbio Health, Inc.
Decision Date2023-04-19
Product CodeFMK
Advisory CommitteeSU
DecisionUnknown
Device Summary
TAP Lancet is a medical device manufactured by Yourbio Health, Inc.. It received FDA 510(k) clearance on 2023-04-19 under approval number K223201. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Unknown.
Frequently Asked Questions
What is the TAP Lancet?
TAP Lancet is a medical device that received FDA 510(k) clearance on 2023-04-19. It is manufactured by Yourbio Health, Inc.. The 510(k) number is K223201.
When was TAP Lancet approved by the FDA?
TAP Lancet received FDA 510(k) clearance on 2023-04-19, under approval number K223201.
What company makes TAP Lancet?
TAP Lancet is manufactured by Yourbio Health, Inc..
What is the FDA product code for TAP Lancet?
The FDA product code for TAP Lancet is FMK.
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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.