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FDA 510(k)

Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4)

K-Number: K241446 · 2024-10-08

ApplicantSichuan Qianii-Beoka Medical Technoiogy Lnc.
Decision Date2024-10-08
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4) is a medical device manufactured by Sichuan Qianii-Beoka Medical Technoiogy Lnc.. It received FDA 510(k) clearance on 2024-10-08 under approval number K241446. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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. It is manufactured by Sichuan Qianii-Beoka Medical Technoiogy Lnc.. The 510(k) number is K241446.

When was Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4) approved by the FDA?

Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4) received FDA 510(k) clearance on 2024-10-08, under approval number K241446.

What company makes Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4)?

Air Compression Massager (ACM-A1, ACM-A2, ACM-A3, ACM-A4) is manufactured by Sichuan Qianii-Beoka Medical Technoiogy Lnc..

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.

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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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