meddevicedb.com FDA Device Reference

Astroglide Sensual Strawberry Personal Lubricant

K213671 Class II Traditional
Decision Date
2022-03-03
Sponsor / Applicant
Biofilm, Inc.

Technical Specification

510(k) Submission ID K213671
Product Code NUC
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2022-03-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Astroglide Sensual Strawberry Personal Lubricant received FDA 510(k) clearance under submission number K213671, sponsored by Biofilm, Inc.. 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 2022-03-03.

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.