meddevicedb.com FDA Device Reference

HYDRAULIC SUCTION BIOPSY PUMP MODEL 7MM

K781038 Class II Traditional
Decision Date
1978-08-14
Sponsor / Applicant
Quinton, Inc.

Technical Specification

510(k) Submission ID K781038
Product Code KNW
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1075
Decision Date 1978-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HYDRAULIC SUCTION BIOPSY PUMP MODEL 7MM received FDA 510(k) clearance under submission number K781038, sponsored by Quinton, 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 1978-08-14.

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.