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AMERICAN CATHETER POLY-SNARE

K940335 Class II Traditional
Decision Date
1994-07-21
Sponsor / Applicant
Intl. Medical, Inc.

Technical Specification

510(k) Submission ID K940335
Product Code FDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4300
Decision Date 1994-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMERICAN CATHETER POLY-SNARE received FDA 510(k) clearance under submission number K940335, sponsored by Intl. Medical, 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 1994-07-21.

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.