meddevicedb.com FDA Device Reference

Omics Core

K190661 Class II Traditional
Decision Date
2019-11-09
Sponsor / Applicant
Nanthealth, Inc.

Technical Specification

510(k) Submission ID K190661
Product Code PZM
Medical Specialty / Panel Pathology
Regulation Citation 21 CFR 866.6080
Decision Date 2019-11-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Omics Core received FDA 510(k) clearance under submission number K190661, sponsored by Nanthealth, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 2019-11-09.

Classification & Regulation

This clearance is catalogued under FDA product code PZM and 21 CFR 866.6080, within the Pathology review panel as a Class II device.