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PROPHYLACTIC (CONDOM) MR. JOHNNY

K865106 Class II Traditional
Decision Date
1987-05-20
Sponsor / Applicant
Medelec Intl. Corp.

Technical Specification

510(k) Submission ID K865106
Product Code HIS
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.5300
Decision Date 1987-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROPHYLACTIC (CONDOM) MR. JOHNNY received FDA 510(k) clearance under submission number K865106, sponsored by Medelec Intl. Corp.. 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 1987-05-20.

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.