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Acuzone Acupuncture Needles, KSC DB Plus Acupuncture Needles

K142760 Class II Traditional
Decision Date
2015-08-25
Sponsor / Applicant
K.S. Choi Corporation

Technical Specification

510(k) Submission ID K142760
Product Code MQX
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5580
Decision Date 2015-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Acuzone Acupuncture Needles, KSC DB Plus Acupuncture Needles received FDA 510(k) clearance under submission number K142760, sponsored by K.S. Choi Corporation. 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 2015-08-25.

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.