meddevicedb.com FDA Device Reference

BIO-DERM COUPLING LOTION

K827885 Class II Traditional
Decision Date
1982-01-29
Sponsor / Applicant
Whs Products, Inc.

Technical Specification

510(k) Submission ID K827885
Product Code HGL
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.2960
Decision Date 1982-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIO-DERM COUPLING LOTION received FDA 510(k) clearance under submission number K827885, sponsored by Whs Products, 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 1982-01-29.

Classification & Regulation

This clearance is catalogued under FDA product code HGL and 21 CFR 884.2960, within the Obstetrics/Gynecology review panel as a Class II device.