The following data is part of a premarket notification filed by Karl Storz Endoscopy with the FDA for Ksea Scbcom.
Device ID | K992469 |
510k Number | K992469 |
Device Name: | KSEA SCBCOM |
Classification | Endoscopic Video Imaging System/component, Gastroenterology-urology |
Applicant | KARL STORZ ENDOSCOPY 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
Contact | Kevin A Kennan |
Correspondent | Kevin A Kennan KARL STORZ ENDOSCOPY 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
Product Code | FET |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-07-26 |
Decision Date | 1999-10-15 |
Summary: | summary |