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Ensizor Endoscopic Scissors

K150939 Class II Traditional
Decision Date
2015-06-08
Sponsor / Applicant
Slater Endoscopy, LLC

Technical Specification

510(k) Submission ID K150939
Product Code OCZ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2015-06-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Ensizor Endoscopic Scissors received FDA 510(k) clearance under submission number K150939, sponsored by Slater Endoscopy, LLC. 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 2015-06-08.

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.