Sterile Lancets for Single Use— 510(k) K242622

Name: FDA 510(k) clearance K242622
Creator: U.S. Food and Drug Administration
Published: 2024-10-28

Substantially Equivalent

Ningbo Caremed Medical Products Co., Ltd.

FDA 510(k) clearance K242622 for Sterile Lancets for Single Use, Substantially Equivalent on 2024-10-28. Applicant: Ningbo Caremed Medical Products Co., Ltd.. Device class: 2.

Clearance details

Applicant: Ningbo Caremed Medical Products Co., Ltd.
Product code: Code QRK
Device class: Class 2
Regulation: 21 CFR 878.4850
Advisory panel: General, Plastic Surgery
Date received: 2024-09-03
Decision date: 2024-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ningbo, CN

Download summary PDF View on FDA.gov ↗

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