meddevicedb.com FDA Device Reference

SecurePortIV Advanced Catheter Securement Adhesive

K223669 Class II Traditional
Decision Date
2023-06-12
Sponsor / Applicant
Adhezion Biomedical, LLC

Technical Specification

510(k) Submission ID K223669
Product Code NZP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4370
Decision Date 2023-06-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SecurePortIV Advanced Catheter Securement Adhesive received FDA 510(k) clearance under submission number K223669, sponsored by Adhezion Biomedical, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2023-06-12.

Classification & Regulation

This clearance is catalogued under FDA product code NZP and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.