The following data is part of a premarket notification filed by Karl Storz Imaging, Inc. with the FDA for Ksi's New Camera Architecture (nca) Video Imaging System.
Device ID | K003325 |
510k Number | K003325 |
Device Name: | KSI'S NEW CAMERA ARCHITECTURE (NCA) VIDEO IMAGING SYSTEM |
Classification | Endoscopic Video Imaging System/component, Gastroenterology-urology |
Applicant | KARL STORZ IMAGING, INC. 175 CREMONA DR. Goleta, CA 93117 |
Contact | Terry Fernandez |
Correspondent | Terry Fernandez KARL STORZ IMAGING, INC. 175 CREMONA DR. Goleta, CA 93117 |
Product Code | FET |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-10-24 |
Decision Date | 2001-04-27 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
04048551337127 | K003325 | 000 |