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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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6 records meeting your search criteria returned- Product Code: JAF Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
THD SPA THD SLIDE ONE 03/12/2020
THD SPA THD DOPPLER PROBE SINGLE USE 07/13/2016
MIZUHO PROBE, DOPPLER 05/04/2016
THD SPA THD REVOLUTION 07/31/2015
THD SPA THD SLIDE DOPPLER PROBE 5 SHOTS NON STER 03/04/2015
THD SPA THD SLIDE OEN STERILE 02/05/2015
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