meddevicedb.com FDA Device Reference

DOBBHOFF(R) POLYPECTOMY SNARE

K901322 Class II Traditional
Decision Date
1990-06-15
Sponsor / Applicant
Biosearch Medical Products, Inc.

Technical Specification

510(k) Submission ID K901322
Product Code FDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 1990-06-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DOBBHOFF(R) POLYPECTOMY SNARE received FDA 510(k) clearance under submission number K901322, sponsored by Biosearch Medical Products, 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 1990-06-15.

Classification & Regulation

This clearance is catalogued under FDA product code FDI and 21 CFR 876.4300, within the Gastroenterology, Urology review panel as a Class II device.