meddevicedb.com FDA Device Reference

WINGED INFUSION SET

K902166 Class II Traditional
Decision Date
1990-08-17
Sponsor / Applicant
Therex Corp.

Technical Specification

510(k) Submission ID K902166
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1990-08-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WINGED INFUSION SET received FDA 510(k) clearance under submission number K902166, sponsored by Therex 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 1990-08-17.

Classification & Regulation

This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.