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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Facet Technologies, LLC. It received FDA 510(k) clearance on 2022-11-28 under 510(k) 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. The listed applicant is Facet Technologies, LLC. The 510(k) number is K223099.

When did Facet Manatee Reusable Lancing Base receive FDA 510(k) clearance?

Facet Manatee Reusable Lancing Base received FDA 510(k) clearance on 2022-11-28, under 510(k) number K223099.

Who is the listed applicant for Facet Manatee Reusable Lancing Base?

The FDA 510(k) record lists Facet Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Facet Manatee Reusable Lancing Base?

The FDA product code for Facet Manatee Reusable Lancing Base is QRL.

Other records listing Facet Technologies, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K232912Facet Aurora Reusable Lancet BaseK223370NeatNick Heel Safety LancetK222539Facet Blood LancetsK221433Facet 28G Universal Lancet

Related Devices (Code: QRL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262211LancetTianjin Huahong Technology Co., Ltd.K260122Lancing Device (PressGo, LDE3, LDE3AST, LDE5, EasyStep)SteriLance Medical (Suzhou), Inc.K253706Lancing device (HH-XV-T)Tianjin Huahong Technology Co., Ltd.K250813MICROLET®NEXT 2 Lancing DeviceAscensia Diabetes Care U.S., Inc.K243306Lancet (IA, IB, IC, ID, IE, IK, IL, IM, IIA, IIB, III, V, VI, VII, VIII, IX); Lancing device (HH-X-T, HH-XV-T, HH-XVI-T, HH-XVII-T, HH-XVIII-T, HH-XIX, HH-XXI-T, HH-XXII-T, HH-XXIII-T, HH-XXIV-T, HH-XXV-T, HH-XXVI-T, HH-XXVIII-T, HH-XXIX-T, HH-XXX-T, HH-XIII-T, HH-XXVII-T)Tianjin Huahong Technology Co., Ltd.K232912Facet Aurora Reusable Lancet BaseFacet Technologies, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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