meddevicedb.com FDA Device Reference

Any-Com Flow

K250823 Class II Special
Decision Date
2025-04-14
Sponsor / Applicant
Mediclus Co., Ltd.

Technical Specification

510(k) Submission ID K250823
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2025-04-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Any-Com Flow received FDA 510(k) clearance under submission number K250823, sponsored by Mediclus Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2025-04-14.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.