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The Sensititre 20 - 24 hour Haemophilus influenzae/Streptococcus pneumoniae (HP) MIC or Breakpoint Susceptibility System with Meropenem in the dilution range of 0.015 - 32 ug/ml.

K242021 Class II Traditional
Decision Date
2024-10-09
Sponsor / Applicant
Thermo Fisher Scientific

Technical Specification

510(k) Submission ID K242021
Product Code JWY
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.1640
Decision Date 2024-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

The Sensititre 20 - 24 hour Haemophilus influenzae/Streptococcus pneumoniae (HP) MIC or Breakpoint Susceptibility System with Meropenem in the dilution range of 0.015 - 32 ug/ml. received FDA 510(k) clearance under submission number K242021, sponsored by Thermo Fisher Scientific. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2024-10-09.

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.