meddevicedb.com FDA Device Reference

DISPOSABLE HEMOSTASIS CHIP

K121505 Class II Traditional
Decision Date
2012-08-31
Sponsor / Applicant
Wilson-Cook Medical Inc./Cook Endoscopy

Technical Specification

510(k) Submission ID K121505
Product Code PKL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4400
Decision Date 2012-08-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE HEMOSTASIS CHIP received FDA 510(k) clearance under submission number K121505, sponsored by Wilson-Cook Medical Inc./Cook Endoscopy. 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 2012-08-31.

Classification & Regulation

This clearance is catalogued under FDA product code PKL and 21 CFR 876.4400, within the Gastroenterology, Urology review panel as a Class II device.