Documento fuente o registro público

FDA 510(k) K231994 — Sensititre 18-24 hour MIC or Breakpoint Susceptibility System with Sulbactam-durlobactam in the dilution range of 0.015/4-32/4 ug/mL

FDA 510(k) index record K231994. Device: Sensititre 18-24 hour MIC or Breakpoint Susceptibility System with Sulbactam-durlobactam in the dilution range of 0.015/4-32/4 ug/mL. Applicant as listed: Thermo Fisher Scientific. Decision date: 2023-08-25.

OtherU.S. Food and Drug Administration (FDA)2023-08-25

Fuente

"device_name": "Sensititre 18-24 hour MIC or Breakpoint Susceptibility System with Sulbactam-durlobactam in the dilution range of 0.015/4-32/4 ug/mL"

Esta entrada describe lo que cubre el documento; el propio documento es la autoridad. Incluirlo no implica estar de acuerdo con sus conclusiones.

Review and references

Reviewer

Automated FDA record verification

Published

2026-10-20

Updated

2026-10-28

Disclaimer

professional use

FDA 510(k) public index record K231994.

Device name: Sensititre 18-24 hour MIC or Breakpoint Susceptibility System with Sulbactam-durlobactam in the dilution range of 0.015/4-32/4 ug/mL. Applicant as listed: Thermo Fisher Scientific.

Decision date: 2023-08-25. Decision wording: Substantially Equivalent.

Product code: JWY. Regulation: 21 CFR 866.1640. Medical specialty: Microbiology.

This page reproduces regulator index metadata. The applicant field identifies the submitter and is not a manufacturer identity check. Consult the original FDA record for the decision and associated documents; this index does not verify current commercial availability or clinical performance.

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