meddevicedb.com FDA Device Reference

allay Nerve Cap (TL5515-1); allay Nerve Cap (TL5515-2); Delivery Tips (TL-7627)

K252051 Class II Traditional
Decision Date
2025-09-29
Sponsor / Applicant
Tulavi Therapeutics, Inc.

Technical Specification

510(k) Submission ID K252051
Product Code SBG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5260
Decision Date 2025-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

allay Nerve Cap (TL5515-1); allay Nerve Cap (TL5515-2); Delivery Tips (TL-7627) received FDA 510(k) clearance under submission number K252051, sponsored by Tulavi Therapeutics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2025-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code SBG and 21 CFR 882.5260, within the Neurology review panel as a Class II device.