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SURGICAL BLADES & SCAPELS (SMPL. W/510K)

K812516 Class I Traditional
Decision Date
1981-10-02
Sponsor / Applicant
Needle Industries(Usa), Inc.

Technical Specification

510(k) Submission ID K812516
Product Code GES
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1981-10-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL BLADES & SCAPELS (SMPL. W/510K) received FDA 510(k) clearance under submission number K812516, sponsored by Needle Industries(Usa), Inc.. 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 1981-10-02.

Classification & Regulation

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