meddevicedb.com FDA Device Reference

SELECT-A-FLOW COLLECTOR

K810645 Class II Traditional
Decision Date
1981-05-05
Sponsor / Applicant
Wenmar Intl. Corp.

Technical Specification

510(k) Submission ID K810645
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1981-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SELECT-A-FLOW COLLECTOR received FDA 510(k) clearance under submission number K810645, sponsored by Wenmar Intl. Corp.. 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 1981-05-05.

Classification & Regulation

This clearance is catalogued under FDA product code KNX and 21 CFR 876.5250, within the Gastroenterology, Urology review panel as a Class II device.