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HAWKINS BREAST LOCALIZATION NEEDLE

K870523 Class I Traditional
Decision Date
1987-03-09
Sponsor / Applicant
N-S Medical Products

Technical Specification

510(k) Submission ID K870523
Product Code GDM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1987-03-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HAWKINS BREAST LOCALIZATION NEEDLE received FDA 510(k) clearance under submission number K870523, sponsored by N-S 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 1987-03-09.

Classification & Regulation

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