meddevicedb.com FDA Device Reference

INTRAVASCULAR CATHETER SECUREMENT DEV

K841487 Class I Traditional
Decision Date
1984-06-28
Sponsor / Applicant
Tapemark Co.

Technical Specification

510(k) Submission ID K841487
Product Code KMK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5210
Decision Date 1984-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTRAVASCULAR CATHETER SECUREMENT DEV received FDA 510(k) clearance under submission number K841487, sponsored by Tapemark Co.. 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 1984-06-28.

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.