Intrelief
K-Number: K211263 · 2021-12-30
Device Summary
Frequently Asked Questions
What is the Intrelief?
Intrelief is a medical device that received FDA 510(k) clearance on 2021-12-30. The listed applicant is Easymed Instruments Co., Ltd.. The 510(k) number is K211263.
When did Intrelief receive FDA 510(k) clearance?
Intrelief received FDA 510(k) clearance on 2021-12-30, under 510(k) number K211263.
Who is the listed applicant for Intrelief?
The FDA 510(k) record lists Easymed Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Intrelief?
The FDA product code for Intrelief is NUH.
Other records listing Easymed Instruments Co., 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: NUH)
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.