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TAI-CHI ACUPUNCTURE NEEDLES

K003760 Class II Traditional
Decision Date
2001-02-06
Sponsor / Applicant
Lhasa Medical, Inc.

Technical Specification

510(k) Submission ID K003760
Product Code MQX
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5580
Decision Date 2001-02-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TAI-CHI ACUPUNCTURE NEEDLES received FDA 510(k) clearance under submission number K003760, sponsored by Lhasa Medical, Inc.. 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 2001-02-06.

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.