meddevicedb.com FDA Device Reference

Robin's Egg

K240689 Class II Traditional
Decision Date
2024-09-17
Sponsor / Applicant
Telebrands Corporation

Technical Specification

510(k) Submission ID K240689
Product Code OAP
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 2024-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Robin's Egg received FDA 510(k) clearance under submission number K240689, sponsored by Telebrands Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2024-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code OAP and 21 CFR 890.5500, within the Physical Medicine review panel as a Class II device.