meddevicedb.com FDA Device Reference

TOP STERILE DISPOS. HYPODERMIC NEEDLES

K832626 Class I Traditional
Decision Date
1983-10-14
Sponsor / Applicant
Top Surgical Manufacturers Co.

Technical Specification

510(k) Submission ID K832626
Product Code GAA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1983-10-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOP STERILE DISPOS. HYPODERMIC NEEDLES received FDA 510(k) clearance under submission number K832626, sponsored by Top Surgical Manufacturers Co.. 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 1983-10-14.

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.