meddevicedb.com FDA Device Reference

BUM Oil

K261905 Class II Traditional
Decision Date
2026-08-07
Sponsor / Applicant
Bumlicious, LLC (DBA “Bumlicious”)

Technical Specification

510(k) Submission ID K261905
Product Code NUC
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2026-08-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BUM Oil received FDA 510(k) clearance under submission number K261905, sponsored by Bumlicious, LLC (DBA “Bumlicious”). The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2026-08-07.

Classification & Regulation

This clearance is catalogued under FDA product code NUC and 21 CFR 884.5300, within the Obstetrics/Gynecology review panel as a Class II device.