510(k) K241627

Device
Safety Lancet (XXXV)
Applicant
Tianjin Huahong Technology Co., Ltd.
510(k) number
K241627
Product code
FMK
Decision
Substantially Equivalent (SESE)
Decision date
2024-06-20
Date received
2024-06-06
Regulation
878.4850
Classification name
Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Ningning Wang
Address
A01, Plant B, # 278, Hangkong Rd., Tianjin Pilot Free Trade Tianjin CN 300308 300308

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code FMK

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