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FRESENIUS STERILE STAY SAFE CAP

K083542 Class II Traditional
Decision Date
2008-12-29
Sponsor / Applicant
Fresenius Medical Care North America

Technical Specification

510(k) Submission ID K083542
Product Code KDJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 2008-12-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FRESENIUS STERILE STAY SAFE CAP received FDA 510(k) clearance under submission number K083542, sponsored by Fresenius Medical Care North America. 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 2008-12-29.

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.