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PENILE CONSTRICTOR RING

K001859 Class II Traditional
Decision Date
2001-01-11
Sponsor / Applicant
Basic Solutions, LLC

Technical Specification

510(k) Submission ID K001859
Product Code LKY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5020
Decision Date 2001-01-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PENILE CONSTRICTOR RING received FDA 510(k) clearance under submission number K001859, sponsored by Basic Solutions, LLC. 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 2001-01-11.

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.