meddevicedb.com FDA Device Reference

Envision ultrasound pad and cover

K190802 Class II Traditional
Decision Date
2019-05-24
Sponsor / Applicant
Civco Medical Solutions

Technical Specification

510(k) Submission ID K190802
Product Code ITX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2019-05-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Envision ultrasound pad and cover received FDA 510(k) clearance under submission number K190802, sponsored by Civco Medical Solutions. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2019-05-24.

Classification & Regulation

This clearance is catalogued under FDA product code ITX and 21 CFR 892.1570, within the Radiology review panel as a Class II device.