meddevicedb.com FDA Device Reference

MTS Eravacycline 0.002 - 32 µg/mL

K182557 Class II Traditional
Decision Date
2018-11-02
Sponsor / Applicant
Liofilchem s.r.l.

Technical Specification

510(k) Submission ID K182557
Product Code JWY
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.1640
Decision Date 2018-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MTS Eravacycline 0.002 - 32 µg/mL received FDA 510(k) clearance under submission number K182557, sponsored by Liofilchem s.r.l.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2018-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code JWY and 21 CFR 866.1640, within the Microbiology review panel as a Class II device.