AngioDynamics, Inc. · Class II · Cleared Aug 1, 2007
| K-number | K071959 |
| Device name | ANGIODYNAMICS, INC.NEVERTOUCH 600UM FIBER AND VENACURE PROCEDURE KIT |
| Applicant | AngioDynamics, Inc. |
| Product code | GEX |
| Device class | Class II |
| Decision date | Aug 1, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 878.4810 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov