meddevicedb.com FDA Device Reference

HS NOTA

K131925 Class II Traditional
Decision Date
2014-10-10
Sponsor / Applicant
H.S. Hospital Services S.P.A.

Technical Specification

510(k) Submission ID K131925
Product Code FCG
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 2014-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HS NOTA received FDA 510(k) clearance under submission number K131925, sponsored by H.S. Hospital Services S.P.A.. 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 2014-10-10.

Classification & Regulation

This clearance is catalogued under FDA product code FCG and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.