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SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY

K874665 Class I Traditional
Decision Date
1988-01-20
Sponsor / Applicant
Precision Dynamics Corp.

Technical Specification

510(k) Submission ID K874665
Product Code LRP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1988-01-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY received FDA 510(k) clearance under submission number K874665, sponsored by Precision Dynamics Corp.. 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 1988-01-20.

Classification & Regulation

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