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GASTRIC SUCTION AND DRAINAGE CATHETER

K002838 Class II Traditional
Decision Date
2001-07-09
Sponsor / Applicant
Bioenterics Corp.

Technical Specification

510(k) Submission ID K002838
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 2001-07-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GASTRIC SUCTION AND DRAINAGE CATHETER received FDA 510(k) clearance under submission number K002838, sponsored by Bioenterics 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 2001-07-09.

Classification & Regulation

This clearance is catalogued under FDA product code KNT and 21 CFR 876.5980, within the Gastroenterology, Urology review panel as a Class II device.