meddevicedb.com FDA Device Reference

OxSAT 100

K191574 Class II Traditional
Decision Date
2020-04-09
Sponsor / Applicant
S.L.P. , Ltd.

Technical Specification

510(k) Submission ID K191574
Product Code DQA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2700
Decision Date 2020-04-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OxSAT 100 received FDA 510(k) clearance under submission number K191574, sponsored by S.L.P. , 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 2020-04-09.

Classification & Regulation

This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.