Mortara Instrument, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mortara Instrument, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Surveyor S2, Surveyor Patient Monitor, Mortara Surveyor Patient Monitor
51
Total
51
Cleared
0
Denied
Mortara Instrument, Inc. has 51 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.
Historical record: 51 cleared submissions from 1983 to 2019.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Mortara Instrument, Inc.
51 devices
Cleared
Jan 24, 2019
Surveyor S2
Cardiovascular
153d
Cleared
Sep 04, 2018
Surveyor Patient Monitor
Cardiovascular
267d
Cleared
CT
Jan 11, 2017
Mortara Surveyor Patient Monitor
Cardiovascular
223d
Cleared
Sep 03, 2016
CardioConfirm
Cardiovascular
99d
Cleared
Aug 04, 2016
Surveyor S4 Mobile Monitor
Cardiovascular
146d
Cleared
Feb 26, 2016
H3+ Holter Recorder
Cardiovascular
164d
Cleared
Jan 06, 2016
Xscribe Stress Exercise Testing Systems, Q-Stress Stress Exercise Testing...
Cardiovascular
92d
Cleared
Dec 03, 2014
SURVEYOR S4 MOBILE MONITOR
Cardiovascular
226d
Cleared
Nov 25, 2014
AMBULO 2400 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM
Cardiovascular
334d
Cleared
Nov 19, 2014
MORTARA MONITORING WAVEFORM VIEWER
Cardiovascular
135d
Cleared
Sep 05, 2014
ELI 380 ELECTROCARDIOGRAPH
Cardiovascular
35d
Cleared
Dec 03, 2013
SURVEYOR CENTRAL STATION
Cardiovascular
159d
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