Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K121480 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Physiological patient monitor. Us... | 2 | 09/04/2014 |
FEI # 3010157426 Spacelabs Healthcare Inc |
| ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Model 96281 is intended for use ... | 2 | 01/30/2014 |
FEI # 3010157426 Spacelabs Healthcare, Llc |
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