Known Identifiers & Locations
FEI Numbers
3015876
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 (0)
No 510(k) notifications found for this entity.
FDA Recall History (2)
| Recall # |
Product Description |
Initiation Date |
Status |
Action |
| Z-0004-06 |
Hard shell carry case for the LIFEPAK 500 AED.
Reason: Some hard shell carry case for LIFEPAK 500 and LIFEPAK CR Plus automated external defibrillators may have blocked pressure vent which may make it difficult to open the case after a sudden decrease in altitude (such as in aircraft landng or mountain descent).
|
2005-07-12 |
Terminated
|
View Details
|
| Z-0005-06 |
Hard shell carry case for the LIFEPAK CR Plus.
Reason: Some hard shell carry case for LIFEPAK 500 and LIFEPAK CR Plus automated external defibrillators may have blocked pressure vent which may make it difficult to open the case after a sudden decrease in altitude (such as in aircraft landng or mountain descent).
|
2005-07-12 |
Terminated
|
View Details
|
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