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CLAVE VIAL ACCESS SPIKE

K934591 Class II Traditional
Decision Date
1994-02-16
Sponsor / Applicant
Icu Medical, Inc.

Technical Specification

510(k) Submission ID K934591
Product Code FMI
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 1994-02-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLAVE VIAL ACCESS SPIKE received FDA 510(k) clearance under submission number K934591, sponsored by Icu 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 1994-02-16.

Classification & Regulation

This clearance is catalogued under FDA product code FMI and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.