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ENTERAL FEEDING TUBE

K890116 Class II Traditional
Decision Date
1989-04-05
Sponsor / Applicant
Hdc Corp.

Technical Specification

510(k) Submission ID K890116
Product Code FPD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 1989-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENTERAL FEEDING TUBE received FDA 510(k) clearance under submission number K890116, sponsored by Hdc 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 1989-04-05.

Classification & Regulation

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