meddevicedb.com FDA Device Reference

BLADE, SCALPEL & BLADE, HANDEL

K954536 Class II Traditional
Decision Date
1995-11-29
Sponsor / Applicant
Access Surgical Intl., Inc.

Technical Specification

510(k) Submission ID K954536
Product Code OCZ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1995-11-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLADE, SCALPEL & BLADE, HANDEL received FDA 510(k) clearance under submission number K954536, sponsored by Access Surgical Intl., 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 1995-11-29.

Classification & Regulation

This clearance is catalogued under FDA product code OCZ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.