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COLORADO CATHETER STERILESURE - NEW NAME PERFIC CATH

K103043 Class II Traditional
Decision Date
2011-01-07
Sponsor / Applicant
Adapta Medical, Inc.

Technical Specification

510(k) Submission ID K103043
Product Code EZD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 2011-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COLORADO CATHETER STERILESURE - NEW NAME PERFIC CATH received FDA 510(k) clearance under submission number K103043, sponsored by Adapta Medical, 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 2011-01-07.

Classification & Regulation

This clearance is catalogued under FDA product code EZD and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.