meddevicedb.com FDA Device Reference

PLASTIC TUBING CONNECTORS

K831920 Class II Traditional
Decision Date
1983-07-19
Sponsor / Applicant
Polymer Technology Corp.

Technical Specification

510(k) Submission ID K831920
Product Code BYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1983-07-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLASTIC TUBING CONNECTORS received FDA 510(k) clearance under submission number K831920, sponsored by Polymer Technology 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 1983-07-19.

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.