meddevicedb.com FDA Device Reference

CONNECTING TUBE

K813228 Class II Traditional
Decision Date
1981-11-27
Sponsor / Applicant
Northern Medical Industries

Technical Specification

510(k) Submission ID K813228
Product Code BYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1981-11-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONNECTING TUBE received FDA 510(k) clearance under submission number K813228, sponsored by Northern Medical Industries. 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 1981-11-27.

Classification & Regulation

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