meddevicedb.com FDA Device Reference

DT Controlled Phototherapy Equipment

K233811 Class II Special
Decision Date
2023-12-13
Sponsor / Applicant
Daavlin Distributing Co.

Technical Specification

510(k) Submission ID K233811
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 2023-12-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DT Controlled Phototherapy Equipment received FDA 510(k) clearance under submission number K233811, sponsored by Daavlin Distributing Co.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2023-12-13.

Classification & Regulation

This clearance is catalogued under FDA product code FTC and 21 CFR 878.4630, within the General, Plastic Surgery review panel as a Class II device.