meddevicedb.com FDA Device Reference

WHS-1000 WOUND HEALING SYSTEM

K050156 Class II Traditional
Decision Date
2005-06-17
Sponsor / Applicant
Iyia Technologies, Inc.

Technical Specification

510(k) Submission ID K050156
Product Code KPJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5650
Decision Date 2005-06-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WHS-1000 WOUND HEALING SYSTEM received FDA 510(k) clearance under submission number K050156, sponsored by Iyia Technologies, 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 2005-06-17.

Classification & Regulation

This clearance is catalogued under FDA product code KPJ and 21 CFR 878.5650, within the General, Plastic Surgery review panel as a Class II device.