meddevicedb.com FDA Device Reference

Etest Ceftaroline (0.002 - 32ug/ml)

K151873 Class II Traditional
Decision Date
2015-10-07
Sponsor / Applicant
Biomerieux S.A.

Technical Specification

510(k) Submission ID K151873
Product Code JWY
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.1640
Decision Date 2015-10-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Etest Ceftaroline (0.002 - 32ug/ml) received FDA 510(k) clearance under submission number K151873, sponsored by Biomerieux S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2015-10-07.

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.