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FDA 510(k)

RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)

K-Number: K240434 · 2024-09-25

ApplicantLi Medical Corporation , Ltd.
Decision Date2024-09-25
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) is a medical device manufactured by Li Medical Corporation , Ltd.. It received FDA 510(k) clearance on 2024-09-25 under approval number K240434. The device is classified under product code HHK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)?

RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) is a medical device that received FDA 510(k) clearance on 2024-09-25. It is manufactured by Li Medical Corporation , Ltd.. The 510(k) number is K240434.

When was RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) approved by the FDA?

RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) received FDA 510(k) clearance on 2024-09-25, under approval number K240434.

What company makes RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)?

RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) is manufactured by Li Medical Corporation , Ltd..

What is the FDA product code for RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)?

The FDA product code for RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) is HHK.

Related Clinical Trials

NCT07592325 Clinical Evaluation of the Access Socket Flexible Socket for Transtibial Prosthesis RECRUITING NCT01082419 Acoustic Radiation Force Impulse Imaging (ARFI) : a New Technique to Assess Liver Elasticity COMPLETED NCT06337292 Incisional Negative Pressure Wound Therapy to Reduce Infection and Complications in High-Risk Fractures RECRUITING NCT06411054 The Efficacy of Acu-TENS as an Adjunct Analgesic During USG-MVA RECRUITING NCT07072598 Comparing Efficiency and Stone-Free Rates Mini PCNL vs Flex URS RECRUITING NCT07527702 Low (-4) vs Physiologic (-8) Pressure Digital Continuous Suction After Lung Resection RECRUITING

Related PubMed Literature

PMID: 31423318 Use of ethylene-oxide gas sterilisation to terminate multidrug-resistant bacterial outbreaks linked to duodenoscopes. BMJ open gastroenterology (2019)

Other Devices by Li Medical Corporation , Ltd.

K240364RELIEEV Uterine Manipulator Injector (CUMI 5.0) K252260RELIEEV HSG Catheter (HSG7FA1)

Related Devices (Code: HHK)

K201952CrossGlide ETS PlusCrossbay Medical K192534CrossBay Endometrial Tissue Sampler (ETS)Crossbay Medical K251882Uterine Aspiration SetGcmedica Enterprise Ltd.(Wuxi)

Official Source

View on FDA Database →

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

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