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PROPORT PLASTIC VENOUS IMPLANTABLE ACCESS SYSTEMS PRE-ASSEMBLED WITH SILICONE CATHETER

K010426 Class II Traditional
Decision Date
2001-03-08
Sponsor / Applicant
Sims Deltec, Inc.

Technical Specification

510(k) Submission ID K010426
Product Code LJT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5965
Decision Date 2001-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROPORT PLASTIC VENOUS IMPLANTABLE ACCESS SYSTEMS PRE-ASSEMBLED WITH SILICONE CATHETER received FDA 510(k) clearance under submission number K010426, sponsored by Sims Deltec, 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 2001-03-08.

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.