Known Identifiers & Locations
FEI Numbers
N/A
Owner Operator Numbers
N/A
Locations Covered
N/A
Registered Establishments (0)
No device registration and listing records found for this entity.
510(k) Premarket Notifications (2)
| Submission # |
Device Name |
Decision Date |
Decision Description |
Action |
| K070372 |
GOPHER 2F SUPPORT CATHETER, MODEL 5600 AND GOPHER 3F SUPPORT CATHETER, MODEL 5610 |
2007-06-01 |
Substantially Equivalent |
View Details
|
| K080022 |
GEL-SPONGE ENT, ABSORBABLE GELATIN SPONGE, USP |
2008-12-09 |
Substantially Equivalent |
View Details
|
FDA Recall History (0)
No recall records found for this entity.
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