meddevicedb.com FDA Device Reference

Tamper Evident Cap

K231095 Class II Traditional
Decision Date
2024-09-04
Sponsor / Applicant
International Medical Industries, Inc.

Technical Specification

510(k) Submission ID K231095
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2024-09-04
Clearance Pathway Traditional

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 K231095, sponsored by International Medical Industries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2024-09-04.

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.