meddevicedb.com FDA Device Reference

Biovitals Analytics Engine

K183282 Class II Traditional
Decision Date
2019-08-15
Sponsor / Applicant
Biofourmis Singapore Pte., Ltd.

Technical Specification

510(k) Submission ID K183282
Product Code PLB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2019-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Biovitals Analytics Engine received FDA 510(k) clearance under submission number K183282, sponsored by Biofourmis Singapore Pte., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2019-08-15.

Classification & Regulation

This clearance is catalogued under FDA product code PLB and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.