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GRANTALDER RHAPSODY ACCESS PORT AND CATHETER

K043178 Class II Traditional
Decision Date
2006-02-02
Sponsor / Applicant
Grantadler Corportation

Technical Specification

510(k) Submission ID K043178
Product Code LJT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5965
Decision Date 2006-02-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GRANTALDER RHAPSODY ACCESS PORT AND CATHETER received FDA 510(k) clearance under submission number K043178, sponsored by Grantadler Corportation. 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 2006-02-02.

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.