meddevicedb.com FDA Device Reference

I.V. TUBING ORGANIZER

K790901 Class II Traditional
Decision Date
1979-06-27
Sponsor / Applicant
Acumed Instruments Corp.

Technical Specification

510(k) Submission ID K790901
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1979-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

I.V. TUBING ORGANIZER received FDA 510(k) clearance under submission number K790901, sponsored by Acumed Instruments 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 1979-06-27.

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.