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ERECXEL ADJUSTABLE PENILE BANDS, CONTREX ADJUSTABLE PENILE BANDS

K993343 Class II Traditional
Decision Date
2000-03-20
Sponsor / Applicant
Erecxel Enterprises

Technical Specification

510(k) Submission ID K993343
Product Code LKY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5020
Decision Date 2000-03-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ERECXEL ADJUSTABLE PENILE BANDS, CONTREX ADJUSTABLE PENILE BANDS received FDA 510(k) clearance under submission number K993343, sponsored by Erecxel Enterprises. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2000-03-20.

Classification & Regulation

This clearance is catalogued under FDA product code LKY and 21 CFR 876.5020, within the Gastroenterology, Urology review panel as a Class II device.