meddevicedb.com FDA Device Reference

Jet Flow Bulk

K242014 Class II Traditional
Decision Date
2024-10-08
Sponsor / Applicant
Meta Biomed Co., Ltd.

Technical Specification

510(k) Submission ID K242014
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2024-10-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Jet Flow Bulk received FDA 510(k) clearance under submission number K242014, sponsored by Meta Biomed Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2024-10-08.

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.