Diversified Medical Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diversified Medical Instruments, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Diversified Medical Instruments, Inc. has 4 FDA 510(k) cleared medical devices. Based in Ellicott City, US.
Historical record: 4 cleared submissions from 1993 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Diversified Medical Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diversified Medical Instruments, Inc.
4 devices
Cleared
May 31, 1994
DMI UTERINE MOBILIZER/ELEVATOR/CANNULA
Obstetrics & Gynecology
418d
Cleared
Feb 25, 1994
DMI LAPAROSCOPIC IRRIGATION PUMP
General & Plastic Surgery
451d
Cleared
May 17, 1993
DMI TOCAR AND CANNULA SYSTEM
General & Plastic Surgery
167d
Cleared
Apr 07, 1993
DMI LAPAROSCOPIC ELECTRODES
General & Plastic Surgery
127d