Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K101148 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| WarmAir Model 135 Convective Warming Device, Cincinnati Sub-Zero Products, Inc. Used to prevent... | 2 | 07/27/2011 |
FEI # 1516825 Cincinnati Sub-Zero Products Inc |
| Operations and Technical Manuals for the firm's WarmAir Model 135 Hyperthermia System (115V, 100V, a... | 2 | 09/01/2011 |
FEI # 1516825 Cincinnati Sub-Zero Products Inc |
-







