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 (1)
| Submission # |
Device Name |
Decision Date |
Decision Description |
Action |
| K092086 |
AMERIGEL WOUND DRESSING PLUS 1/2 OZ. (15G TUBE), MODEL A2025; 1 OZ. (30G TUBE), MODEL A2026; 3 OZ (90G TUBE),MODEL A2027 |
2009-07-30 |
Substantially Equivalent |
View Details
|
FDA Recall History (0)
No recall records found for this entity.
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