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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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85 records meeting your search criteria returned- Product Code: KDQ Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
ATRIUM MEDICAL CORPORATION OCEAN CHEST DRAIN 07/15/2020
ATRIUM MEDICAL CORPORATION OCEAN DRAIN 07/15/2020
ATRIUM MEDICAL CORPORATION OCEAN CHEST DRAIN 07/15/2020
ATRIUM MEDICAL CORPORATION OCEAN CHEST DRAIN 07/15/2020
ATRIUM MEDICAL CORPORATION OCEAN CHEST DRAIN 07/15/2020
ATRIUM MEDICAL CORPORATION OCEAN DRAIN 07/15/2020
ATRIUM MEDICAL CORPORATION DRAINS OCEAN DOUBLE 07/15/2020
TELEFLEX MEDICAL PE SAHARA DRY SUCT/DRY SEAL LF 6/CS 07/13/2020
DEROYAL INDUSTRIES, INC. 2500CC CANISTER, 2 ELBOW 07/01/2020
DEROYAL INDUSTRIES, INC. 2500CC CANISTER, 2 ELBOW 07/01/2020
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