meddevicedb.com FDA Device Reference

SWAN NECK PRESTERNAL PERITONEAL DIALYSIS CATHETER

K950042 Class II Traditional
Decision Date
1995-12-15
Sponsor / Applicant
Accurate Surgical Instruments Co.

Technical Specification

510(k) Submission ID K950042
Product Code FJS
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 1995-12-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SWAN NECK PRESTERNAL PERITONEAL DIALYSIS CATHETER received FDA 510(k) clearance under submission number K950042, sponsored by Accurate Surgical Instruments Co.. 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 1995-12-15.

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.