meddevicedb.com FDA Device Reference

CW-DISPOSABLE ACUPUNCTURE NEEDLE

K962419 Class II Traditional
Decision Date
1996-07-25
Sponsor / Applicant
Acupuncture Supplies Import Co.

Technical Specification

510(k) Submission ID K962419
Product Code MQX
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5580
Decision Date 1996-07-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CW-DISPOSABLE ACUPUNCTURE NEEDLE received FDA 510(k) clearance under submission number K962419, sponsored by Acupuncture Supplies Import Co.. 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 1996-07-25.

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.