Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K052573 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Stardust Flexible Y Sensor Probe model number 612054. Filter, mask, and/or accessories for sleep t... | 2 | 04/24/2008 |
FEI # 2518422 Respironics, Inc. |
| Breathing Frequency Monitor Stardust 2 Domestic model number 1025720. Filter, mask, and/or accesso... | 2 | 04/24/2008 |
FEI # 2518422 Respironics, Inc. |
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