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PERITONEAL DIALYSIS STYSTEM AND ACCESSORIES

K900295 Class II Traditional
Decision Date
1990-11-21
Sponsor / Applicant
Microwave Medical Systems, Inc.

Technical Specification

510(k) Submission ID K900295
Product Code KDJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 1990-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERITONEAL DIALYSIS STYSTEM AND ACCESSORIES received FDA 510(k) clearance under submission number K900295, sponsored by Microwave Medical Systems, Inc.. 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 1990-11-21.

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.