meddevicedb.com FDA Device Reference

Tamper Evident Cap

K193192 Class II Special
Decision Date
2020-01-31
Sponsor / Applicant
International Medical Industries, Inc.

Technical Specification

510(k) Submission ID K193192
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2020-01-31
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tamper Evident Cap received FDA 510(k) clearance under submission number K193192, sponsored by International Medical Industries, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2020-01-31.

Classification & Regulation

This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.