Medical Device Recalls
-
|
1 to 10 of 23 Results
510(K) Number: K080927 |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| BrightView SPECT, Model Number 882480 | 2 | 07/22/2019 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| BrightView X , Model Number 882478 | 2 | 07/22/2019 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| BrightView X upgraded to XCT 882454 | 2 | 02/10/2017 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| BrightView X, Gamma Camera, Product Code 882478 | 2 | 01/05/2024 |
FEI # 3006648320 Philips North America |
| BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit format 4535... | 1 | 02/02/2024 |
FEI # 3006648320 Philips North America |
| BrightView XCT | 2 | 02/10/2017 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| BrightView XCT & BrightView XCT Upgrade, gamma cameras; For Single Proton Emission Computed Tomograp... | 2 | 02/26/2016 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| BrightView XCT (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray syst... | 2 | 06/11/2015 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| BrightView XCT , Model Number 882482 | 2 | 07/22/2019 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
| BrightView XCT Gamma Camera, 3/4". Philips Medical Systems, Inc. Intended to produce images depi... | 2 | 08/04/2011 |
FEI # 1525965 Philips Medical Systems |
-







