Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K982635 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Nicolet® Elite® 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended ... | 2 | 07/13/2017 | Natus Neurology Inc |
| Nicolet® Elite® 5 MHz Vascular Probe, Model #: X1L004, Catalog Code: N500. Intended for non-invas... | 2 | 07/13/2017 | Natus Neurology Inc |
| Nicolet® Elite® 3 MHz OB Probe, Model #: X1L001, Catalog Code: N300. Intended for non-invasive su... | 2 | 07/13/2017 | Natus Neurology Inc |
| Nicolet® Elite® 2 MHz OB Water Proof Probe, Model #: X1L008, Catalog Code: NW20. Intended for non... | 2 | 07/13/2017 | Natus Neurology Inc |
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