FDA 510(k) clearance · back to tracker

Air compression massager (ACM-C1, ACM-C2, ACM-C3, ACM-C4, ACM-C5, ACM-C6, ACM-C7, ACM-C8, ACM-C9, ACM-5C1, ACM-5C2, ACM-5C3, ACM-5C4, ACM-5C5, ACM-5C6, ACM-5C7, ACM-5C8, ACM-5C9)

Sichuan Qianli-Beoka Medical Technology, Inc. cleared K262812 on 2026-10-05, decision: substantially equivalent

K-number

K262812

Sponsor

Sichuan Qianli-Beoka Medical Technology, Inc.

Device

Air compression massager (ACM-C1, ACM-C2, ACM-C3, ACM-C4, ACM-C5, ACM-C6, ACM-C7, ACM-C8, ACM-C9, ACM-5C1, ACM-5C2, ACM-5C3, ACM-5C4, ACM-5C5, ACM-5C6, ACM-5C7, ACM-5C8, ACM-5C9)

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-10-05

Product code

IRP

Advisory committee

Physical Medicine

Medical specialty

Physical Medicine

Regulation number

890.5650

Official FDA record

Open K262812on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.