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 (3)
| Submission # |
Device Name |
Decision Date |
Decision Description |
Action |
| K851403 |
VENTREZYME ALLERGEN DATA REDUCTION SYSTEM |
1985-06-21 |
Substantially Equivalent |
View Details
|
| K880678 |
MODIFIED VENTRESCREEN BETA HCG ENZYME IMMUNOASSAY |
1988-04-05 |
Substantially Equivalent |
View Details
|
| K905612 |
VENTREX COATED TUBE IGE RADIOIMMUNOASSAY |
1991-02-21 |
Substantially Equivalent |
View Details
|
FDA Recall History (0)
No recall records found for this entity.
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