Delphi Consulting Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Delphi Consulting Group - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Delphi Consulting Group has 6 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 6 cleared submissions from 1996 to 1999. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Delphi Consulting Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Delphi Consulting Group
6 devices
Cleared
Apr 28, 1999
TRINITY II SINGLE CHAMBER DVT PUMP
Cardiovascular
190d
Cleared
Nov 04, 1997
TRINITY DVT SYSTEM
Cardiovascular
398d
Cleared
Aug 06, 1997
TRINITY SLEEVES, HUNTLEIGH PUMP COMPATIBLE(T.B.D.)
Cardiovascular
216d
Cleared
Dec 09, 1996
SIMULSCOPE AUSCULTATION AND SIMULSCOPE BEDSIDE AUSCULTATION SYSTEM
Cardiovascular
203d
Cleared
Jun 11, 1996
E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120
Cardiovascular
68d
Cleared
Feb 22, 1996
TRINITY SLEEVE(S)
Cardiovascular
148d