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KARL STORZ VIDEO FLEXIBLE VIDEO ENT ENDOSCOPE SYSTEM

K071530 Class II Traditional
Decision Date
2007-08-24
Sponsor / Applicant
KARL STORZ Endoscopy-America, Inc.

Technical Specification

510(k) Submission ID K071530
Product Code EOQ
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4680
Decision Date 2007-08-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KARL STORZ VIDEO FLEXIBLE VIDEO ENT ENDOSCOPE SYSTEM received FDA 510(k) clearance under submission number K071530, sponsored by KARL STORZ Endoscopy-America, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2007-08-24.

Classification & Regulation

This clearance is catalogued under FDA product code EOQ and 21 CFR 874.4680, within the Ear, Nose, Throat review panel as a Class II device.