FDA.reportPublic FDA data

MAUDE MDR 8778123

MDR report key
8778123
Report number
3019216-2019-00042
Event key
0
Event type
3
Date received
2019-07-10
Adverse event
3
Product problem
3
Patients in event
0
Reporter occupation
401
Health professional
3
Initial report to FDA
3
Event location
3

Manufacturer Contact#

Contact
MR. PAUL CORRIGAN
Address
22100 BOTHELL EVERETT HIGHWAY BOTHELL WA 98021 US
Phone
425-425-4254
Report source
M
Manufacturer link flag
Y

Devices#

Seq, Brand, Generic table
SeqBrandGenericManufacturerProduct codeModelCatalogLotPMA510(k)ImplantEvaluatedAvailability
1EPIQ 7C - 795201SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC22PHILIPS ULTRASOUND, INCIYNEPIQ 7C - 795201EPIQ 7C - 795201US118B1262N Y

Patients#

Sequence, Received, Treatment table
SequenceReceivedTreatmentOutcome
12019-07-100

Event Narratives#

No narrative records found.