meddevicedb.com FDA Device Reference

HYPODERMIC & SUTURE NEEDLES

K813256 Class II Traditional
Decision Date
1982-03-25
Sponsor / Applicant
Needle Industries(Usa), Inc.

Technical Specification

510(k) Submission ID K813256
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 1982-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HYPODERMIC & SUTURE NEEDLES received FDA 510(k) clearance under submission number K813256, sponsored by Needle Industries(Usa), Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1982-03-25.

Classification & Regulation

This clearance is catalogued under FDA product code FMI and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.