meddevicedb.com FDA Device Reference

XSTAT 30, 3-PACK, XSTAT 30, 1-PACK

K152624 Class II Traditional
Decision Date
2015-12-07
Sponsor / Applicant
Revmedx, Inc.

Technical Specification

510(k) Submission ID K152624
Product Code PGZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4452
Decision Date 2015-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

XSTAT 30, 3-PACK, XSTAT 30, 1-PACK received FDA 510(k) clearance under submission number K152624, sponsored by Revmedx, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2015-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code PGZ and 21 CFR 878.4452, within the General, Plastic Surgery review panel as a Class II device.