meddevicedb.com FDA Device Reference

MOSS(R) STEEL BREAKAWAY(R) INTRODUCER

K945480 Class II Traditional
Decision Date
1995-08-28
Sponsor / Applicant
Harry A. Schlakman

Technical Specification

510(k) Submission ID K945480
Product Code KOB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5090
Decision Date 1995-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MOSS(R) STEEL BREAKAWAY(R) INTRODUCER received FDA 510(k) clearance under submission number K945480, sponsored by Harry A. Schlakman. 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 1995-08-28.

Classification & Regulation

This clearance is catalogued under FDA product code KOB and 21 CFR 876.5090, within the Gastroenterology, Urology review panel as a Class II device.