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TUBE FEEDING SET

K810573 Class II Traditional
Decision Date
1981-04-23
Sponsor / Applicant
Harvard Laboratories

Technical Specification

510(k) Submission ID K810573
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 1981-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TUBE FEEDING SET received FDA 510(k) clearance under submission number K810573, sponsored by Harvard Laboratories. 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 1981-04-23.

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.