510(k) K240434

Device
RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)
Applicant
Li Medical Corporation , Ltd.
510(k) number
K240434
Product code
HHK
Decision
Substantially Equivalent (SESE)
Decision date
2024-09-25
Date received
2024-02-14
Regulation
884.1175
Classification name
Curette, Suction, Endometrial (And Accessories)
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Jago Chen
Address
2f., # 43, Zhongxing Rd. New Taipei City TW 221012 221012

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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