Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K080603 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Ultrasound needles, 22G (0.7 mm) x 50mm, packaged individually, 10 needles/box, item number REF USC0... | 2 | 05/12/2014 |
FEI # 3005379387 RM Temena GmbH |
| Ultrasound USB needles, with 30 degree bevel, packaged individually, 10 needles/box, item number RE... | 2 | 05/12/2014 |
FEI # 3005379387 RM Temena GmbH |
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