Delphi Consulting Group
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K983680 | TRINITY II SINGLE CHAMBER DVT PUMP | JOW | 1999-04-28 | View |
| 510(k) | K963957 | TRINITY DVT SYSTEM | JOW | 1997-11-04 | View |
| 510(k) | K970014 | TRINITY SLEEVES, HUNTLEIGH PUMP COMPATIBLE(T.B.D.) | JOW | 1997-08-06 | View |
| 510(k) | K961937 | SIMULSCOPE AUSCULTATION AND SIMULSCOPE BEDSIDE AUSCULTATION SYSTEM | DQD | 1996-12-09 | View |
| 510(k) | K961301 | E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120 | DQD | 1996-06-11 | View |
| 510(k) | K954489 | TRINITY SLEEVE(S) | JOW | 1996-02-22 | View |
No matching devices.
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