meddevicedb.com FDA Device Reference

SOLUTION ADMINISTRATION SET

K860541 Class II Traditional
Decision Date
1986-03-25
Sponsor / Applicant
Travenol Laboratories, S.A.

Technical Specification

510(k) Submission ID K860541
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1986-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOLUTION ADMINISTRATION SET received FDA 510(k) clearance under submission number K860541, sponsored by Travenol Laboratories, S.A.. 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 1986-03-25.

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.