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KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG)

K896605 Class I Traditional
Decision Date
1990-01-04
Sponsor / Applicant
National-Standard Medical Products

Technical Specification

510(k) Submission ID K896605
Product Code GAA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1990-01-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG) received FDA 510(k) clearance under submission number K896605, sponsored by National-Standard Medical Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1990-01-04.

Classification & Regulation

This clearance is catalogued under FDA product code GAA and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.