Cardiva Medical, Inc. · Class II · Cleared Mar 22, 2007
| K-number | K070485 |
| Device name | BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58L |
| Applicant | Cardiva Medical, Inc. |
| Product code | DXC |
| Device class | Class II |
| Decision date | Mar 22, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 870.4450 |
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