Mesa Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mesa Medical, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Mesa Medical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1982 to 1994. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Mesa Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mesa Medical, Inc.
7 devices
Cleared
Jan 25, 1994
90DX MULTITEST METER, MODIFICATION
Gastroenterology & Urology
475d
Cleared
Aug 11, 1988
MODEL 90DX MULTITEST METER
Gastroenterology & Urology
87d
Cleared
Mar 24, 1987
MODEL 102 PH METER
Gastroenterology & Urology
21d
Cleared
Sep 10, 1985
RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANT
Gastroenterology & Urology
75d
Cleared
Oct 04, 1984
WAREXIN RECOMMENDED ALTERNATIVE DIALYZ
Gastroenterology & Urology
27d
Cleared
Mar 23, 1984
ECHO MM1000
Gastroenterology & Urology
98d
Cleared
Jun 23, 1982
ECHO, MODEL MM-1000
Gastroenterology & Urology
44d