Aptus Endosystems, Inc.
Aptus Endosystems, Inc. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2014.
Top product codes for Aptus Endosystems, Inc.
Recent clearances by Aptus Endosystems, Inc.
- K140036 — APTUS HELI-FX GUIDE - 22CM DEFLECTABLE LENGTH; APTUS HELI-FX GUIDE - 28CM DEFLECTABLE LENGTH; APTUS HELI-FX APPLIER WITH
- K130677 — APTUS HELI-FX AORTIC SECUREMENT SYSTEM
- K121168 — APTUS 18FR HELIFX GUIDE-22 DEFLECTABLE LENGTH
- DEN100026 — APTUS STEERABLE ENDOGUIDE WITH OBTURATOR, APTUS ENDOSTAPLE APPLIER WITH ENDOSTAPLE CASSETTE, APTUS ENDOSTAPLE CASSETTE
Data sourced from openFDA. This site is unofficial and independent of the FDA.