Diamond Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diamond Medical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Diamond Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Saint Paul, US.
Historical record: 6 cleared submissions from 1987 to 1992. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Diamond Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diamond Medical, Inc.
6 devices
Cleared
Dec 03, 1992
DMI BLOOD GAS ANALYZER/CARTRIDGE
Chemistry
71d
Cleared
Jan 08, 1992
DMI BLOD GAS ANALYZER/CARTRIDGE
Chemistry
57d
Cleared
Feb 08, 1988
DIAMOND MEDICAL, INC. MODEL DM 800
Gastroenterology & Urology
88d
Cleared
Feb 08, 1988
DIAMOND MEDICAL, INC. MODEL DM 600
Gastroenterology & Urology
88d
Cleared
Feb 05, 1988
MODEL ISO-2001 UNIV. PATIENT ISOLATION CIRCUIT
Gastroenterology & Urology
36d
Cleared
Mar 17, 1987
DIAMOND MEDICAL, INC., MODEL DM 700
Gastroenterology & Urology
204d