meddevicedb.com FDA Device Reference

POWER INJECTABLE IMPLANTABLE INFUSION PORT WITH SILICONE LUMEN (ATTACHABLE AND PRE-ATTACHED)

K070003 Class II Traditional
Decision Date
2007-05-15
Sponsor / Applicant
Medcomp

Technical Specification

510(k) Submission ID K070003
Product Code LJT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5965
Decision Date 2007-05-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWER INJECTABLE IMPLANTABLE INFUSION PORT WITH SILICONE LUMEN (ATTACHABLE AND PRE-ATTACHED) received FDA 510(k) clearance under submission number K070003, sponsored by Medcomp. 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 2007-05-15.

Classification & Regulation

This clearance is catalogued under FDA product code LJT and 21 CFR 880.5965, within the General Hospital review panel as a Class II device.