Ascent Healthcare Solutions
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 21
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K111600 | REPROCESSED HAND ACTIVATE SEALER/DIVIDER | November 15, 2011 |
| K110189 | REPROCESSED ELECTROSURGICAL INSTRUMENT | July 18, 2011 |
| K100909 | REPROCESSED COMPRESSION SLEEVES | July 23, 2010 |
| K100254 | REPROCESSED CS BI-DIECTIONAL DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER | May 28, 2010 |
| K100537 | REPROCESSED ULTRASONIC CURVED SHEARS WITH TORQUE WRENCH AND GRIP ASSIST MODEL FCS9, TWBLUE, GABLUE | May 12, 2010 |
| K100080 | REPROCESSED TROCARS, MODEL B5LT AND CB5LT | March 19, 2010 |
| K093702 | REPROCESSED ULTRASONIC COAGULATING SHEARS | March 4, 2010 |
| K092425 | REPROCESSED 3D DIAGNOSTIC ULTRASOUND CATHETERS, MODEL SNDSTR10 | October 21, 2009 |
| K090323 | REPROCESSED ELECTROPHYSIOLOGY CATHETERS | April 1, 2009 |
| K082023 | REPROCESSED ELECTROPHYSIOLOGY CATHETERS | September 16, 2008 |
| K081238 | REPROCESSED MASIMO PULSE OXIMETER SENSORS | July 29, 2008 |
| K081329 | REPROCESSED ELECTROPHYSIOLOGY CATHETERS | July 9, 2008 |
| K063788 | REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS | October 15, 2007 |
| K070059 | REPROCESSED TROCARS | October 2, 2007 |
| K070034 | REPROCESSED GUIDANT CARDIAC STABILIZATION AND POSITIONING DEVICES | August 17, 2007 |
| K070036 | REPROCESSED MEDTRONIC CARDIAC STABILIZATION AND POSITIONING DEVICES | August 17, 2007 |
| K062525 | REPROCESSED LIGASURE VESSEL SEALER/DIVIDER | May 16, 2007 |
| K063076 | REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER | March 29, 2007 |
| K062497 | REPROCESSED TROCARS | January 31, 2007 |
| K053585 | VANGUARD REPROCESSED SUTURE PASSER | October 11, 2006 |