meddevicedb.com FDA Device Reference

KARL STORZ CONTACT NASAL MICRO-ENDOSCOPES

K972855 Class II Traditional
Decision Date
1997-09-08
Sponsor / Applicant
KARL STORZ Endoscopy-America, Inc.

Technical Specification

510(k) Submission ID K972855
Product Code EOB
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4760
Decision Date 1997-09-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KARL STORZ CONTACT NASAL MICRO-ENDOSCOPES received FDA 510(k) clearance under submission number K972855, 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 1997-09-08.

Classification & Regulation

This clearance is catalogued under FDA product code EOB and 21 CFR 874.4760, within the Ear, Nose, Throat review panel as a Class II device.