RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)
K-Number: K240434 · 2024-09-25
Device Summary
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. The listed applicant is Li Medical Corporation , Ltd.. The 510(k) number is K240434.
When did RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) receive FDA 510(k) clearance?
RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) received FDA 510(k) clearance on 2024-09-25, under 510(k) number K240434.
Who is the listed applicant for RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)?
The FDA 510(k) record lists Li Medical Corporation , Ltd. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Li Medical Corporation , Ltd. 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.
Related Devices (Code: HHK)
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.
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.