meddevicedb.com FDA Device Reference

JJ SKINNER CAREKITS(TM) DIALYSIS ON/OFF KIT

K925469 Class I Traditional
Decision Date
1995-05-03
Sponsor / Applicant
J.J. Skinner, Inc.

Technical Specification

510(k) Submission ID K925469
Product Code FKG
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1995-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JJ SKINNER CAREKITS(TM) DIALYSIS ON/OFF KIT received FDA 510(k) clearance under submission number K925469, sponsored by J.J. Skinner, 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 1995-05-03.

Classification & Regulation

This clearance is catalogued under FDA product code FKG and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class I device.