meddevicedb.com FDA Device Reference

CCPD 3 LITER DRAINAGE SET

K810671 Class II Traditional
Decision Date
1981-03-24
Sponsor / Applicant
American Medical Products, Inc.

Technical Specification

510(k) Submission ID K810671
Product Code KDJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 1981-03-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CCPD 3 LITER DRAINAGE SET received FDA 510(k) clearance under submission number K810671, sponsored by American Medical Products, 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 1981-03-24.

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.