Documento fuente o registro público

FDA 510(k) K192118 — CRP Vario

FDA 510(k) index record K192118. Device: CRP Vario. Applicant as listed: SENTINEL CH. SpA. Decision date: 2019-11-08.

OtherU.S. Food and Drug Administration (FDA)2019-11-08

Fuente

"device_name": "CRP Vario"
api.fda.gov · Consultado el 2026-10-19

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

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Reviewer

Automated FDA record verification

Published

2026-10-20

Updated

2026-10-20

Disclaimer

professional use

References

FDA 510(k) public index record K192118.

Device name: CRP Vario. Applicant as listed: SENTINEL CH. SpA.

Decision date: 2019-11-08. Decision wording: Substantially Equivalent.

Product code: DCK. Regulation: 21 CFR 866.5270. Medical specialty: Immunology.

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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FDA 510(k) K192118 — CRP Vario

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