meddevicedb.com FDA Device Reference

TRAY AND BAG, CATHETERIZATION

K790271 Class II Traditional
Decision Date
1979-03-06
Sponsor / Applicant
Snyder Laboratories, Inc.

Technical Specification

510(k) Submission ID K790271
Product Code FCM
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 1979-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRAY AND BAG, CATHETERIZATION received FDA 510(k) clearance under submission number K790271, sponsored by Snyder Laboratories, 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 1979-03-06.

Classification & Regulation

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