Aptus Endosystems
Aptus Endosystems appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 16, 2014.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K141041 | APTUS HELI-FX ANCILLARY ENDOANCHOR CASSETTE | May 16, 2014 |
| K140036 | APTUS HELI-FX GUIDE - 22CM DEFLECTABLE LENGTH; APTUS HELI-FX GUIDE - 28CM DEFLECTABLE LENGTH; APTUS | February 6, 2014 |
| K130677 | APTUS HELI-FX AORTIC SECUREMENT SYSTEM | April 12, 2013 |
| K121168 | APTUS 18FR HELIFX GUIDE-22 DEFLECTABLE LENGTH | August 8, 2012 |
| DEN100026 | APTUS STEERABLE ENDOGUIDE WITH OBTURATOR, APTUS ENDOSTAPLE APPLIER WITH ENDOSTAPLE CASSETTE, APTUS E | November 21, 2011 |