Facet 28G Universal Lancet— 510(k) K221433

Name: FDA 510(k) clearance K221433
Creator: U.S. Food and Drug Administration
Published: 2022-07-15

Substantially Equivalent

Facet Technologies, LLC

FDA 510(k) clearance K221433 for Facet 28G Universal Lancet, Substantially Equivalent on 2022-07-15. Applicant: Facet Technologies, LLC. Device class: 2.

Clearance details

Applicant: Facet Technologies, LLC
Product code: Code QRK
Device class: Class 2
Regulation: 21 CFR 878.4850
Advisory panel: General, Plastic Surgery
Date received: 2022-05-17
Decision date: 2022-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Atlanta, GA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.