The following data is part of a premarket notification filed by Brainlab, Ag with the FDA for Advanced Viewer.
Device ID | K132763 |
510k Number | K132763 |
Device Name: | ADVANCED VIEWER |
Classification | System, Image Processing, Radiological |
Applicant | BRAINLAB, AG KAPELLENSTR. 12 Feldkirchen, DE 85622 |
Contact | Alexander Schwiersch |
Correspondent | Alexander Schwiersch BRAINLAB, AG KAPELLENSTR. 12 Feldkirchen, DE 85622 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-09-04 |
Decision Date | 2014-02-28 |
Summary: | summary |