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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K190124
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Brand Name: CLEANER BOTTLE Product Name: CLEANER BOTTLE Model/Catalog Number: EG-1000 Software Ve... 2 04/24/2024 FEI # 3002806910
Electro Medical Systems SA
Brand Name: PIEZON Bottle Product Name: PIEZON Bottle Model/Catalog Number: EG-111 Software Versi... 2 04/24/2024 FEI # 3002806910
Electro Medical Systems SA
Brand Name: WATER BOTTLE Product Name: WATER BOTTLE Model/Catalog Number: EG-121 Software Version... 2 04/24/2024 FEI # 3002806910
Electro Medical Systems SA
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