The following data is part of a premarket notification filed by Karl Storz Imaging, Inc. with the FDA for Karl Storz Endovision Xl Endoscopic Camera System.
Device ID | K974391 |
510k Number | K974391 |
Device Name: | KARL STORZ ENDOVISION XL ENDOSCOPIC CAMERA SYSTEM |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | KARL STORZ IMAGING, INC. 175 CREMONA DR. Goleta, CA 93117 |
Contact | Terry F Ernandez |
Correspondent | Terry F Ernandez KARL STORZ IMAGING, INC. 175 CREMONA DR. Goleta, CA 93117 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-11-21 |
Decision Date | 1998-01-30 |
Summary: | summary |