Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K133810 |
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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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| VC150 Vital Signs Monitor (VC150 monitor equipped with Masimo SpO2 technique only); Innokas Medical ... | 2 | 01/28/2015 |
FEI # 3007615597 INNOKAS MEDICAL OY |
| CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's vital signs at the site ... | 2 | 08/19/2016 |
FEI # 3007615597 INNOKAS MEDICAL OY |
| CARESCAPE VC150 Vital Signs Monitor Monitor vital signs in humans | 2 | 11/11/2015 |
FEI # 3007615597 Innokas Medical Oy |
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