meddevicedb.com FDA Device Reference

PROSTATIC ASPIRATION BIOPSY SET

K870735 Class II Traditional
Decision Date
1987-03-25
Sponsor / Applicant
Van-Tec, Inc.

Technical Specification

510(k) Submission ID K870735
Product Code KNW
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 1987-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROSTATIC ASPIRATION BIOPSY SET received FDA 510(k) clearance under submission number K870735, sponsored by Van-Tec, Inc.. 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 1987-03-25.

Classification & Regulation

This clearance is catalogued under FDA product code KNW and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.