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5F DIGNITY CT TITANIUM PORT

K130923 Class II Traditional
Decision Date
2013-07-31
Sponsor / Applicant
Medical Components, Inc.

Technical Specification

510(k) Submission ID K130923
Product Code LJT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5965
Decision Date 2013-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

5F DIGNITY CT TITANIUM PORT received FDA 510(k) clearance under submission number K130923, sponsored by Medical Components, 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 2013-07-31.

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.