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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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391 records meeting your search criteria returned- Product Code: DQA Report Date From: 1/1/2023 Report Date To: 12/31/2023

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ManufacturerBrand NameDate Report Received
NELLCOR PURITAN BENNETT MEXICO SA NELLCOR 12/15/2023
NELLCOR PURITAN BENNETT MEXICO SA NELLCOR OXYSOFT 12/15/2023
NELLCOR PURITAN BENNETT MEXICO SA NELLCOR 12/15/2023
NELLCOR PURITAN BENNETT MEXICO SA NELLCOR 12/13/2023
MEDIANA CO. LTD. NELLCOR 12/12/2023
MEDIANA CO. LTD. NELLCOR 12/12/2023
MEDIANA CO. LTD. NELLCOR 12/11/2023
APK TECHNOLOGY CO., LTD. PULSE OXIMETER SENSOR 12/08/2023
MEDIANA CO. LTD. NELLCOR 12/07/2023
MASIMO - 15750 ALTON PKWY RADICAL-7 HANDHELD 12/07/2023
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