Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K113380 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Prostiva RF Therapy Hand Piece Kit, REF 8929, Rx only, sterilized using Ethylene Oxide. The Prost... | 2 | 11/08/2013 | Urologix, Inc. |
Medtronic Prostiva RF Therapy Generator. The Prostiva RF system is indicated for the treatment of... | 2 | 04/02/2013 | Medtronic Neuromodulation |
-