NeatNick Heel Safety Lancet
K-Number: K223370 · 2023-02-13
ApplicantFacet Technologies, LLC
Decision Date2023-02-13
Product CodeFMK
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
NeatNick Heel Safety Lancet is a medical device manufactured by Facet Technologies, LLC. It received FDA 510(k) clearance on 2023-02-13 under approval number K223370. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the NeatNick Heel Safety Lancet?
NeatNick Heel Safety Lancet is a medical device that received FDA 510(k) clearance on 2023-02-13. It is manufactured by Facet Technologies, LLC. The 510(k) number is K223370.
When was NeatNick Heel Safety Lancet approved by the FDA?
NeatNick Heel Safety Lancet received FDA 510(k) clearance on 2023-02-13, under approval number K223370.
What company makes NeatNick Heel Safety Lancet?
NeatNick Heel Safety Lancet is manufactured by Facet Technologies, LLC.
What is the FDA product code for NeatNick Heel Safety Lancet?
The FDA product code for NeatNick Heel Safety Lancet is FMK.
Other Devices by Facet Technologies, LLC
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K193009Promisemed Heel Blood LancetPromisemed Hangzhou Meditech Co., Ltd.
K192666Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety LancetPromisemed Hangzhou Meditech Co., Ltd.
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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.