meddevicedb.com FDA Device Reference

WINGED INFUSION SET

K832622 Class II Traditional
Decision Date
1983-10-14
Sponsor / Applicant
Top Surgical Manufacturers Co.

Technical Specification

510(k) Submission ID K832622
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1983-10-14
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 K832622, sponsored by Top Surgical Manufacturers Co.. 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 1983-10-14.

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.