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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K202517
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Product Description
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Recall
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FDA Recall
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ellacor System with Micro-Coring Technology-Indicated for use by medical professionals for the treat... 2 08/11/2023 FEI # 3020704367
Cytrellis Biosystems, Inc.
Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring System System intended for... 2 05/26/2023 FEI # 3020704367
Cytrellis Biosystems, Inc.
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