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KARL STORZ KNIVES, CURETTES

K945686 Class II Traditional
Decision Date
1995-02-13
Sponsor / Applicant
KARL STORZ Endoscopy-America, Inc.

Technical Specification

510(k) Submission ID K945686
Product Code EZO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4770
Decision Date 1995-02-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KARL STORZ KNIVES, CURETTES received FDA 510(k) clearance under submission number K945686, sponsored by KARL STORZ Endoscopy-America, 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 1995-02-13.

Classification & Regulation

This clearance is catalogued under FDA product code EZO and 21 CFR 876.4770, within the Gastroenterology, Urology review panel as a Class II device.