Class Class II

Robin’s Egg (K240689)

K240689 2024-09-17 Traditional
Home/ Devices/ Robin’s Egg (K240689)

Description

Robin's Egg by Telebrands Corporation, an FDA 510(k) cleared physical medicine device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240689
Clearance Date2024-09-17
Clearance TypeTraditional
Product CodeOAP
Regulation Number890.5500

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote

Predicate lineage for K240689

A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Robin’s Egg (K240689) cites 1 predicate device and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K173729REVIAN REDPhotonmd, Inc.2018

Trace the full predicate network for K240689

A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.

Scroll to Top