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SHAMROCK SAFETY WINGED INFUSION SET

K895481 Class II Traditional
Decision Date
1989-10-10
Sponsor / Applicant
Ryan Medical, Inc.

Technical Specification

510(k) Submission ID K895481
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1989-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHAMROCK SAFETY WINGED INFUSION SET received FDA 510(k) clearance under submission number K895481, sponsored by Ryan Medical, Inc.. 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 1989-10-10.

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.