Facet Manatee Reusable Lancing Base
K-Number: K223099 · 2022-11-28
ApplicantFacet Technologies, LLC
Decision Date2022-11-28
Product CodeQRL
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Facet Manatee Reusable Lancing Base is a medical device manufactured by Facet Technologies, LLC. It received FDA 510(k) clearance on 2022-11-28 under approval number K223099. The device is classified under product code QRL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Facet Manatee Reusable Lancing Base?
Facet Manatee Reusable Lancing Base is a medical device that received FDA 510(k) clearance on 2022-11-28. It is manufactured by Facet Technologies, LLC. The 510(k) number is K223099.
When was Facet Manatee Reusable Lancing Base approved by the FDA?
Facet Manatee Reusable Lancing Base received FDA 510(k) clearance on 2022-11-28, under approval number K223099.
What company makes Facet Manatee Reusable Lancing Base?
Facet Manatee Reusable Lancing Base is manufactured by Facet Technologies, LLC.
What is the FDA product code for Facet Manatee Reusable Lancing Base?
The FDA product code for Facet Manatee Reusable Lancing Base is QRL.
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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.