Delphi Medical Systems is one of 18365 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Delphi Medical Systems - FDA 510(k) Cleared Devices
Recent clearances: DELPHI INFUSION PUMP/ DELPHI ADMINISTRATION SET MODEL IV-01000/ MODEL IV-02XXXX (WHERE X IS ANY NUMBER BETWEEN 0-9), PORTABLE OXYGEN CONCENTRATOR, MODEL RS-00400
2
Total
2
Cleared
0
Denied
Delphi Medical Systems has 2 FDA 510(k) cleared medical devices. Based in Troy, US.
Historical record: 2 cleared submissions from 2008 to 2009. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Delphi Medical Systems Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Delphi Medical Systems
2 devices