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GE Inspection Technologies, LP

9 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus recall (Z-2236-2016)GE Inspection Technologies, LP2016-07-23
GE Optional Laser Centering Device X-ray generator. recall (Z-2320-2015)GE Inspection Technologies, LP2015-08-13
GE Inspection Technologies x|tome|x L240 an Cabinet X-ray system recall (Z-1211-2015)GE Inspection Technologies, LP2015-03-20
GE Inspection Technologies x|argos 160D system. Cabinet x-ray system. recall (Z-1225-2015)GE Inspection Technologies, LP2015-03-20
GE Cabinet X-ray systems recall (Z-0426-2015)GE Inspection Technologies, LP2014-12-17
Phoenix x/ray analyser series. Phoenix x|ray analyser series cabinet x-ray systems are use recall (Z-1825-2011)GE Inspection Technologies, LP2011-04-06
Phoenix x/ray inspector series. Phoenix x|ray inspector series cabinet x-ray systems are u recall (Z-1826-2011)GE Inspection Technologies, LP2011-04-06
Phoenix x/ray v/tome/x series. Phoenix x|ray v|tome|x series cabinet x-ray systems are use recall (Z-1827-2011)GE Inspection Technologies, LP2011-04-06
Phoenix x/ray nanotom series. Phoenix x|ray nanotom series cabinet x-ray systems are used recall (Z-1828-2011)GE Inspection Technologies, LP2011-04-06

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Every clearance here is in the API, with alerts when new ones post.