meddevicedb.com FDA Device Reference

IV TRANSFER SPIKE

K943095 Class II Traditional
Decision Date
1994-09-30
Sponsor / Applicant
Migada, Ltd.

Technical Specification

510(k) Submission ID K943095
Product Code LHI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 1994-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IV TRANSFER SPIKE received FDA 510(k) clearance under submission number K943095, sponsored by Migada, Ltd.. 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 1994-09-30.

Classification & Regulation

This clearance is catalogued under FDA product code LHI and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.