Del Mar Avionics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Del Mar Avionics - FDA 510(k) Cleared Devices
Recent clearances: OMNICORDER, MODEL 464, SENTINEL RECORDER, MODELS 471/472, HOLTER DIGICORDER WITH PACER OPTION (MODEL 483)
54
Total
54
Cleared
0
Denied
Del Mar Avionics has 54 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 54 cleared submissions from 1977 to 1999.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Del Mar Avionics
54 devices
Cleared
Feb 09, 1999
OMNICORDER, MODEL 464
Cardiovascular
35d
Cleared
Dec 30, 1997
SENTINEL RECORDER, MODELS 471/472
Cardiovascular
236d
Cleared
Mar 13, 1997
HOLTER DIGICORDER WITH PACER OPTION (MODEL 483)
Cardiovascular
211d
Cleared
Aug 17, 1995
HOLTER PACERCORDER(R)
Cardiovascular
225d
Cleared
May 10, 1995
HOLTER SSR DIGICORDER(TM)
Cardiovascular
341d
Cleared
Apr 21, 1993
SPRINT DX, MODEL 5400 EXERCISE STRESS TEST SYSTEM
Cardiovascular
344d
Cleared
Apr 18, 1990
MODEL 263 SPECTRASCAN(TM) HOLTER ANALYSIS SYSTEM
Cardiovascular
133d
Cleared
Feb 13, 1990
MICROPOTENTIAL ANALYZER/SPECTROCARDIOGRAPHY OPTION
Cardiovascular
138d
Cleared
Feb 08, 1990
MODEL 493 SSR-3 THREE CHANNEL SOLID-STATE RECORDER
Cardiovascular
203d
Cleared
May 11, 1989
MODEL 152 DELTA HOLTER ECG ANALYSIS SYSTEM
Cardiovascular
69d
Cleared
Feb 06, 1989
MODEL 499 SSR ANALYSIS SYSTEM
Cardiovascular
76d
Cleared
Jan 05, 1989
MODEL 463 ELECTROCARDIORECORDER RECORDER
Cardiovascular
83d
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