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MILLENNIA ACUPUNCTURE NEEDLE

K001718 Class II Traditional
Decision Date
2000-06-21
Sponsor / Applicant
United Pacific Co., Ltd.

Technical Specification

510(k) Submission ID K001718
Product Code MQX
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5580
Decision Date 2000-06-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MILLENNIA ACUPUNCTURE NEEDLE received FDA 510(k) clearance under submission number K001718, sponsored by United Pacific Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2000-06-21.

Classification & Regulation

This clearance is catalogued under FDA product code MQX and 21 CFR 880.5580, within the General Hospital review panel as a Class II device.