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SURFLO WINGED INFUSION SET WITH NEEDLE PROTECTION (SURSHIELD)

K072894 Class II Special
Decision Date
2007-11-06
Sponsor / Applicant
Terumo Europe N.V.

Technical Specification

510(k) Submission ID K072894
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2007-11-06
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURFLO WINGED INFUSION SET WITH NEEDLE PROTECTION (SURSHIELD) received FDA 510(k) clearance under submission number K072894, sponsored by Terumo Europe N.V.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2007-11-06.

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.