Carl Zeiss Surgical GmbH
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K110590 | INTRABEAM NEEDLE APPLICATOR | April 13, 2012 |
| K100468 | ZEISS INFRARED 800 WITH FLOW 800 OPTION | March 3, 2010 |
| K090584 | INTRABEAM SYSTEM WITH BALLOON APPLICATOR AND CBG SETS | November 24, 2009 |
| K051055 | INTRABEAM SYSTEM | May 23, 2005 |