Medical Device Recalls
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1 result found
510(K) Number: K041607 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Q-Tel. The Q-Tel RMS system is a computer-based cardiac and pulmonary rehabilitation data acquisitio... | 2 | 04/29/2020 | WELCH ALLYN, INC/MORTARA |
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