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EZ-FIX I.V. CATHETER HOLDER

K821796 Class I Traditional
Decision Date
1982-06-24
Sponsor / Applicant
Dyna Care

Technical Specification

510(k) Submission ID K821796
Product Code KMK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5210
Decision Date 1982-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EZ-FIX I.V. CATHETER HOLDER received FDA 510(k) clearance under submission number K821796, sponsored by Dyna Care. 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 1982-06-24.

Classification & Regulation

This clearance is catalogued under FDA product code KMK and 21 CFR 880.5210, within the General Hospital review panel as a Class I device.