meddevicedb.com FDA Device Reference

Tamper Evident Cap For use with ENFit Syringes

K170672 Class II Traditional
Decision Date
2017-10-06
Sponsor / Applicant
International Medical Industries, Inc.

Technical Specification

510(k) Submission ID K170672
Product Code PNR
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 2017-10-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tamper Evident Cap For use with ENFit Syringes received FDA 510(k) clearance under submission number K170672, sponsored by International Medical Industries, 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 2017-10-06.

Classification & Regulation

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