meddevicedb.com FDA Device Reference

TUBE, STERILE CONDUCTIVE CONNECTING

K760202 Class II Traditional
Decision Date
1976-07-19
Sponsor / Applicant
Ipco Corp.

Technical Specification

510(k) Submission ID K760202
Product Code GAZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1976-07-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TUBE, STERILE CONDUCTIVE CONNECTING received FDA 510(k) clearance under submission number K760202, sponsored by Ipco Corp.. 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 1976-07-19.

Classification & Regulation

This clearance is catalogued under FDA product code GAZ and 21 CFR 880.6740, within the General Hospital review panel as a Class II device.