meddevicedb.com FDA Device Reference

PhenoMATRIX

K251511 Class II Traditional
Decision Date
2026-01-22
Sponsor / Applicant
Copan Wasp Srl

Technical Specification

510(k) Submission ID K251511
Product Code PPU
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.2190
Decision Date 2026-01-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PhenoMATRIX received FDA 510(k) clearance under submission number K251511, sponsored by Copan Wasp Srl. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2026-01-22.

Classification & Regulation

This clearance is catalogued under FDA product code PPU and 21 CFR 866.2190, within the Microbiology review panel as a Class II device.