Medical Device Recalls
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1 result found
510(K) Number: K120088 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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mcompass 2-channel Balloon Catheters The mcompass Biofeedback Anorectal Manometry System is for u... | 2 | 08/25/2017 | Medspira, Llc |
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