Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4)
K-Number: K241446 · 2024-10-08
Device Summary
Frequently Asked Questions
What is the Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4)?
Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4) is a medical device that received FDA 510(k) clearance on 2024-10-08. The listed applicant is Sichuan Qianii-Beoka Medical Technoiogy Lnc.. The 510(k) number is K241446.
When did Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4) receive FDA 510(k) clearance?
Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4) received FDA 510(k) clearance on 2024-10-08, under 510(k) number K241446.
Who is the listed applicant for Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4)?
The FDA 510(k) record lists Sichuan Qianii-Beoka Medical Technoiogy Lnc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4)?
The FDA product code for Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4) is IRP.
Related Devices (Code: IRP)
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.