Hart Enterprises, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Hart Enterprises, Inc. has 4 FDA 510(k) cleared medical devices. Based in Wyoming, US.
Historical record: 4 cleared submissions from 1988 to 1993. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hart Enterprises, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Hart Enterprises, Inc.
4 devices
Cleared
Aug 26, 1993
PENCIL POINT SPINAL NEEDLE
Anesthesiology
505d
Cleared
Oct 30, 1991
AUTOMATED BIOPSY DEVICE, MODIFICATION
General & Plastic Surgery
65d
Cleared
Jan 26, 1989
NEEDLE INSERT FOR SOFT TISSUE BIOPSY DEVICE
General & Plastic Surgery
42d
Cleared
May 13, 1988
BREAST LOCALIZATION NEEDLES
General & Plastic Surgery
21d