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KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM

K990154 Class I Traditional
Decision Date
1999-06-01
Sponsor / Applicant
Karl Storz Imaging, Inc.

Technical Specification

510(k) Submission ID K990154
Product Code FWF
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4160
Decision Date 1999-06-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM received FDA 510(k) clearance under submission number K990154, sponsored by Karl Storz Imaging, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1999-06-01.

Classification & Regulation

This clearance is catalogued under FDA product code FWF and 21 CFR 878.4160, within the General, Plastic Surgery review panel as a Class I device.