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CHEMO-CATH INTRAPERITONEAL CATHETER

K863819 Class II Traditional
Decision Date
1987-02-04
Sponsor / Applicant
Hdc Corp.

Technical Specification

510(k) Submission ID K863819
Product Code FJS
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 1987-02-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHEMO-CATH INTRAPERITONEAL CATHETER received FDA 510(k) clearance under submission number K863819, sponsored by Hdc Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1987-02-04.

Classification & Regulation

This clearance is catalogued under FDA product code FJS and 21 CFR 876.5630, within the Gastroenterology, Urology review panel as a Class II device.