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JOE LUB HELMET CONDOM

K011378 Class II Abbreviated
Decision Date
2002-03-25
Sponsor / Applicant
Marketing Sales Concepts, Inc. (Msci)

Technical Specification

510(k) Submission ID K011378
Product Code HIS
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 2002-03-25
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JOE LUB HELMET CONDOM received FDA 510(k) clearance under submission number K011378, sponsored by Marketing Sales Concepts, Inc. (Msci). The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2002-03-25.

Classification & Regulation

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