meddevicedb.com FDA Device Reference

PERITONEAL DIALYSIS ADMIN. SET

K780082 Class II Traditional
Decision Date
1978-01-24
Sponsor / Applicant
Physio-Control Corp.

Technical Specification

510(k) Submission ID K780082
Product Code KDJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 1978-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERITONEAL DIALYSIS ADMIN. SET received FDA 510(k) clearance under submission number K780082, sponsored by Physio-Control 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 1978-01-24.

Classification & Regulation

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